A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022301



Internal ID19111519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119932900..119998067hg38UCSC Ensembl
Innerchr7:119572954..119638121hg19UCSC Ensembl
Innerchr7:119360190..119425357hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3865168
hg1965168
hg1865168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6601n100
Supporting Variantsnssv3662104, nssv3662106, nssv3662103, nssv3662105
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022301
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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