A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528843



Internal ID15109450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180606292..180647248hg38UCSC Ensembl
Innerchr5:180033292..180074248hg19UCSC Ensembl
Innerchr5:179965898..180006854hg18UCSC Ensembl
Innerchr5:179965898..180006854hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3840957
hg1940957
hg1840957
hg1740957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705520
Samples
Known GenesFLT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528843
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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