A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525194



Internal ID15105801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95020696..95084938hg38UCSC Ensembl
Innerchr13:95672950..95737192hg19UCSC Ensembl
Innerchr13:94470951..94535193hg18UCSC Ensembl
Innerchr13:94470951..94535193hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3864243
hg1964243
hg1864243
hg1764243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701275
Samples
Known GenesABCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525194
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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