A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026764



Internal ID19115982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159178468..159324697hg38UCSC Ensembl
Innerchr7:158971159..159117386hg19UCSC Ensembl
Innerchr7:158663920..158810147hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38146230
hg19146228
hg18146228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6776n100
Supporting Variantsnssv3674796
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)nsv1026764
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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