A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526318



Internal ID15453611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:118875140..118885894hg38UCSC Ensembl
Innerchr5:118210835..118221589hg19UCSC Ensembl
Innerchr5:118238734..118249488hg18UCSC Ensembl
Innerchr5:118238734..118249488hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3810755
hg1910755
hg1810755
hg1710755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702604
Samples
Known GenesDTWD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526318
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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