A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015415



Internal ID18757949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143755783..143875193hg38UCSC Ensembl
Innerchr7:143452876..143572286hg19UCSC Ensembl
Innerchr7:143083809..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38119411
hg19119411
hg18119411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6712n100
Supporting Variantsnssv3754817
Samples
Known GenesCTAGE6, FAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015415
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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