A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645776



Internal ID6685837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38267218..38288767hg38UCSC Ensembl
Innerchr20:38267218..38288767hg38UCSC Ensembl
Outerchr20:38266718..38289267hg38UCSC Ensembl
chr20:36895620..36917169hg19UCSC Ensembl
Innerchr20:36895620..36917169hg19UCSC Ensembl
Outerchr20:36895120..36917669hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3821550
hg1921550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16180423
SamplesHG03619
Known GenesLOC149684
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645776
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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