A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705548



Internal ID15095514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160039744..160062448hg38UCSC Ensembl
Innerchr5:159466751..159489455hg19UCSC Ensembl
Innerchr5:159399329..159422033hg18UCSC Ensembl
Innerchr5:159399329..159422033hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3822705
hg1922705
hg1822705
hg1722705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528868
Supporting Variants
Samples
Known GenesTTC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705548
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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