A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053621



Internal ID19142840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43604052..43703678hg38UCSC Ensembl
Innerchr15:43896250..43995876hg19UCSC Ensembl
Innerchr15:41683542..41783168hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3899627
hg1999627
hg1899627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2585n100
Supporting Variantsnssv3552324, nssv3716717
Samples
Known GenesCATSPER2, CKMT1A, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053621
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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