A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036938



Internal ID18779469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71655767..71980514hg38UCSC Ensembl
Innerchr15:71948106..72272855hg19UCSC Ensembl
Innerchr15:69735160..70059909hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38324748
hg19324750
hg18324750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717959
Samples
Known GenesMYO9A, NR2E3, THSD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036938
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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