A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701832



Internal ID15438484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:30373475..30374604hg38UCSC Ensembl
Innerchr13:30947612..30948741hg19UCSC Ensembl
Innerchr13:29845612..29846741hg18UCSC Ensembl
Innerchr13:29845612..29846741hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381130
hg191130
hg181130
hg171130
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525675
Supporting Variants
Samples
Known GenesLINC00426
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701832
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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