A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636267



Internal ID7023063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42428800..42431444hg38UCSC Ensembl
Innerchr15:42428999..42431373hg38UCSC Ensembl
Outerchr15:42428634..42431610hg38UCSC Ensembl
chr15:42720998..42723642hg19UCSC Ensembl
Innerchr15:42721197..42723571hg19UCSC Ensembl
Outerchr15:42720832..42723808hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231010, essv15231014, essv15231020, essv15231008, essv15231003, essv15231016, essv15230995, essv15231019, essv15230996, essv15231000, essv15231012, essv15231002, essv15231018, essv15231005, essv15231001, essv15230998, essv15230999, essv15231017, essv15231004, essv15230997, essv15231007, essv15231011, essv15231013, essv15231006, essv15231009, essv15231015, essv15230994
SamplesHG03514, NA19394, NA18861, HG02973, HG03193, HG02769, NA19235, HG03267, NA19025, HG03055, HG03169, HG02977, HG02439, NA18934, NA19462, HG02757, NA19035, HG04219, NA18909, NA20276, HG02010, HG03458, HG03279, HG03410, NA19213, NA18522, HG02629
Known GenesZNF106
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636267
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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