A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522703



Internal ID15103310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:64384387..64583407hg38UCSC Ensembl
Innerchr3:64370063..64569083hg19UCSC Ensembl
Innerchr3:64345103..64544123hg18UCSC Ensembl
Innerchr3:64345103..64544123hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38199021
hg19199021
hg18199021
hg17199021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv289n21
Supporting Variantsnssv706115
Samples
Known GenesADAMTS9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522703
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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