A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015945



Internal ID18758479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76443262..76674181hg38UCSC Ensembl
Innerchr7:76072579..76303498hg19UCSC Ensembl
Innerchr7:75910515..76141434hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38230920
hg19230920
hg18230920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6471n100
Supporting Variantsnssv3656500, nssv3656499
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015945
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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