A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705132



Internal ID15095098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180614662..180636743hg38UCSC Ensembl
Innerchr5:180041662..180063743hg19UCSC Ensembl
Innerchr5:179974268..179996349hg18UCSC Ensembl
Innerchr5:179974268..179996349hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3822082
hg1922082
hg1822082
hg1722082
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528522
Supporting Variants
Samples
Known GenesFLT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705132
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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