A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13037700



Internal ID3917752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155823681..155830402hg38UCSC Ensembl
Innerchr7:155823721..155830363hg38UCSC Ensembl
Outerchr7:155823642..155830442hg38UCSC Ensembl
chr7:155616375..155623096hg19UCSC Ensembl
Innerchr7:155616415..155623057hg19UCSC Ensembl
Outerchr7:155616336..155623136hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg386722
hg196722
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615638
Supporting Variants
SamplesHG03571
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13037700
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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