A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999583



Internal ID19159120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108832182..108939054hg38UCSC Ensembl
Innerchr3:108551029..108657901hg19UCSC Ensembl
Innerchr3:110033719..110140591hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38106873
hg19106873
hg18106873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4834n100
Supporting Variantsnssv3735246
Samples
Known GenesGUCA1C, TRAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999583
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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