A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517541



Internal ID15098148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40265067..40303426hg38UCSC Ensembl
Innerchr15:40557268..40595627hg19UCSC Ensembl
Innerchr15:38344560..38382919hg18UCSC Ensembl
Innerchr15:38344560..38382919hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3838360
hg1938360
hg1838360
hg1738360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692799, nssv660429, nssv656052, nssv677810, nssv678807, nssv652307, nssv688330, nssv668844, nssv692537, nssv669798, nssv671568, nssv667247, nssv685331
Samples
Known GenesANKRD63, PAK6, PLCB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517541
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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