A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038991



Internal ID18781522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43622539..43732292hg38UCSC Ensembl
Innerchr15:43914737..44024490hg19UCSC Ensembl
Innerchr15:41702029..41811782hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38109754
hg19109754
hg18109754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2586n100
Supporting Variantsnssv3552328, nssv3552327, nssv3716718, nssv3552329
Samples
Known GenesCATSPER2, CKMT1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038991
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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