A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524098



Internal ID8418373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58528779..58542192hg38UCSC Ensembl
Innerchr15:58820978..58834391hg19UCSC Ensembl
Innerchr15:56608270..56621683hg18UCSC Ensembl
Innerchr15:56608270..56621683hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3813414
hg1913414
hg1813414
hg1713414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699973
Samples
Known GenesLIPC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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