A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614047



Internal ID6654254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88137786..88140082hg38UCSC Ensembl
Innerchr7:88137812..88140057hg38UCSC Ensembl
Outerchr7:88137761..88140108hg38UCSC Ensembl
chr7:87767101..87769397hg19UCSC Ensembl
Innerchr7:87767127..87769372hg19UCSC Ensembl
Outerchr7:87767076..87769423hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382297
hg192297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12879882, essv12879883
SamplesHG03985, HG04144
Known GenesADAM22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614047
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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