A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523315



Internal ID15450608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101663675..101708975hg38UCSC Ensembl
Innerchr15:102203878..102249178hg19UCSC Ensembl
Innerchr15:100021401..100066701hg18UCSC Ensembl
Innerchr15:100021401..100066701hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3845301
hg1945301
hg1845301
hg1745301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699057
Samples
Known GenesTARSL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523315
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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