A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031955



Internal ID19121177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143802282hg38UCSC Ensembl
Innerchr7:143223069..143499375hg19UCSC Ensembl
Innerchr7:142933191..143130308hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38276307
hg19276307
hg18197118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670241, nssv3670242
Samples
Known GenesCTAGE15, CTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031955
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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