A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520932



Internal ID15101539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135090535..135102557hg38UCSC Ensembl
Innerchr3:134809377..134821399hg19UCSC Ensembl
Innerchr3:136292067..136304089hg18UCSC Ensembl
Innerchr3:136292075..136304097hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3812023
hg1912023
hg1812023
hg1712023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697695
Samples
Known GenesEPHB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520932
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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