A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019171



Internal ID19108389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143747426hg38UCSC Ensembl
Innerchr7:143223069..143444519hg19UCSC Ensembl
Innerchr7:142933191..143075452hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38221451
hg19221451
hg18142262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6701n100
Supporting Variantsnssv3670239
Samples
Known GenesCTAGE15, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019171
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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