A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022413



Internal ID18764947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143881082hg38UCSC Ensembl
Innerchr7:143223069..143578175hg19UCSC Ensembl
Innerchr7:142933191..143209108hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38355107
hg19355107
hg18275918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n100
Supporting Variantsnssv3670308, nssv3670309
Samples
Known GenesCTAGE15, CTAGE6, FAM115A, 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)nsv1022413
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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