A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033726



Internal ID19122947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143835893hg38UCSC Ensembl
Innerchr7:143223069..143532986hg19UCSC Ensembl
Innerchr7:142933191..143163919hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38309918
hg19309918
hg18230729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670272, nssv3670273, nssv3670280, nssv3670283, nssv3670282, nssv3670259, nssv3754731, nssv3670266, nssv3670260, nssv3670278, nssv3670264, nssv3670265, nssv3670269, nssv3670267, nssv3670258, nssv3670268, nssv3754727, nssv3670274, nssv3670270, nssv3670279, nssv3670277, nssv3754730, nssv3670275, nssv3670276, nssv3670263, nssv3670257, nssv3670281, nssv3754728, nssv3670262, nssv3670261, nssv3670271, nssv3754729
Samples
Known GenesCTAGE15, CTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033726
Frequency
Sample Size11257
Observed Gain32
Observed Loss0
Observed Complex0
Frequencyn/a


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