A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979755



Internal ID12980691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16212129..16278002hg38UCSC Ensembl
Innerchr7:16251754..16317627hg19UCSC Ensembl
Innerchr7:16218279..16284152hg18UCSC Ensembl
Innerchr7:16024994..16090867hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3865874
hg1965874
hg1865874
hg1765874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34298
Supporting Variants
SamplesNA18621
Known GenesISPD, ISPD-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979755
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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