A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049654



Internal ID19138873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64843547..64960198hg38UCSC Ensembl
Innerchr15:65135746..65252540hg19UCSC Ensembl
Innerchr15:62922799..63039593hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38116652
hg19116795
hg18116795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717952
Samples
Known GenesANKDD1A, PLEKHO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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