A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965825



Internal ID15913095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77291901..77295527hg38UCSC Ensembl
Innerchr3:77341052..77344678hg19UCSC Ensembl
Innerchr3:77423742..77427368hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383627
hg193627
hg183627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590732
Supporting Variants
Samples
Known GenesROBO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv965825
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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