A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999606



Internal ID19159143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96566227..96608620hg38UCSC Ensembl
Innerchr3:96285071..96327464hg19UCSC Ensembl
Innerchr3:97767761..97810154hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3842394
hg1942394
hg1842394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4817n100
Supporting Variantsnssv3603317, nssv3735181
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999606
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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