A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592982



Internal ID16380391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195113211..195213905hg38UCSC Ensembl
Innerchr3:194833940..194934634hg19UCSC Ensembl
Innerchr3:196315229..196415923hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38100695
hg19100695
hg18100695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv986719
Samples
Known GenesXXYLT1, XXYLT1-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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