A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483085



Internal ID15582198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:93499132..93666365hg38UCSC Ensembl
Innerchr13:94151385..94318618hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38167234
hg19167234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996370
Samples
Known GenesGPC6
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483085
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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