A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694557



Internal ID15431209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73070057..73071858hg38UCSC Ensembl
Innerchr13:73644195..73645996hg19UCSC Ensembl
Innerchr13:72542196..72543997hg18UCSC Ensembl
Innerchr13:72542196..72543997hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381802
hg191802
hg181802
hg171802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521789
Supporting Variants
Samples
Known GenesKLF5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694557
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer