A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703475



Internal ID15093441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151498616..151525837hg38UCSC Ensembl
Innerchr5:150878177..150905398hg19UCSC Ensembl
Innerchr5:150858370..150885591hg18UCSC Ensembl
Innerchr5:150858370..150885591hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3827222
hg1927222
hg1827222
hg1727222
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527096
Supporting Variants
Samples
Known GenesFAT2, MIR6499
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703475
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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