A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523153



Internal ID15450446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87801824..87818882hg38UCSC Ensembl
Innerchr13:88454079..88471137hg19UCSC Ensembl
Innerchr13:87252080..87269138hg18UCSC Ensembl
Innerchr13:87252080..87269138hg17UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3817059
hg1917059
hg1817059
hg1717059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698861
Samples
Known GenesLINC00397
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523153
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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