A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022261



Internal ID19111479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159214650..159324628hg38UCSC Ensembl
Innerchr7:159007339..159117317hg19UCSC Ensembl
Innerchr7:158700100..158810078hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38109979
hg19109979
hg18109979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6779n100
Supporting Variantsnssv3674807
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)nsv1022261
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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