A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979770



Internal ID12980722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153832191..153960395hg38UCSC Ensembl
Innerchr7:153529276..153657480hg19UCSC Ensembl
Innerchr7:153160209..153288413hg18UCSC Ensembl
Innerchr7:152966924..153095128hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38128205
hg19128205
hg18128205
hg17128205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34787
Supporting Variants
SamplesNA18623
Known GenesDPP6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979770
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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