A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705861



Internal ID15095827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96433165..96532034hg38UCSC Ensembl
Innerchr13:97085419..97184288hg19UCSC Ensembl
Innerchr13:95883420..95982289hg18UCSC Ensembl
Innerchr13:95883420..95982289hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3898870
hg1998870
hg1898870
hg1798870
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522493
Supporting Variants
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705861
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