A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152884



Internal ID15874333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195096755..195241159hg38UCSC Ensembl
Innerchr3:194817484..194961888hg19UCSC Ensembl
Innerchr3:196298773..196443177hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38144405
hg19144405
hg18144405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592981
Supporting Variants
SamplesHGDP00525
Known GenesXXYLT1, XXYLT1-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152884
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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