A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703741



Internal ID15440393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108331662..108337350hg38UCSC Ensembl
Innerchr13:108984010..108989698hg19UCSC Ensembl
Innerchr13:107782011..107787699hg18UCSC Ensembl
Innerchr13:107782011..107787699hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385689
hg195689
hg185689
hg175689
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527316
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703741
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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