A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999796



Internal ID19159332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:79713311..79889013hg38UCSC Ensembl
Innerchr3:79762461..79938163hg19UCSC Ensembl
Innerchr3:79845151..80020853hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38175703
hg19175703
hg18175703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596228
Samples
Known GenesROBO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999796
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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