A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660429



Internal ID15050395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40265863..40291963hg38UCSC Ensembl
Innerchr15:40558064..40584164hg19UCSC Ensembl
Innerchr15:38345356..38371456hg18UCSC Ensembl
Innerchr15:38345356..38371456hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3826101
hg1926101
hg1826101
hg1726101
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517541
Supporting Variants
Samples
Known GenesANKRD63, PAK6, PLCB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660429
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer