A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700744



Internal ID15437396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85290164..85498872hg38UCSC Ensembl
Innerchr13:85864299..86073007hg19UCSC Ensembl
Innerchr13:84762300..84971008hg18UCSC Ensembl
Innerchr13:84762300..84971008hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38208709
hg19208709
hg18208709
hg17208709
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524753
Supporting Variants
Samples
Known GenesLINC00351
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700744
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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