A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636142



Internal ID7022938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35752575..35753331hg38UCSC Ensembl
Innerchr15:35752586..35753320hg38UCSC Ensembl
Outerchr15:35752564..35753342hg38UCSC Ensembl
chr15:36044776..36045532hg19UCSC Ensembl
Innerchr15:36044787..36045521hg19UCSC Ensembl
Outerchr15:36044765..36045543hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15214217, essv15214218, essv15214219
SamplesHG01051, HG01676, NA19720
Known GenesDPH6-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636142
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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