A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024013



Internal ID19113230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143549301..143816712hg38UCSC Ensembl
Innerchr7:143246394..143513805hg19UCSC Ensembl
Innerchr7:142956516..143144738hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38267412
hg19267412
hg18188223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670387, nssv3670386, nssv3670388
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)nsv1024013
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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