A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525852



Internal ID15453145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65972842..65978483hg38UCSC Ensembl
Innerchr5:65268670..65274311hg19UCSC Ensembl
Innerchr5:65304426..65310067hg18UCSC Ensembl
Innerchr5:65304426..65310067hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385642
hg195642
hg185642
hg175642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702046
Samples
Known GenesERBB2IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525852
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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