A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv721191



Internal ID16015147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109025141..109031762hg38UCSC Ensembl
Innerchr1:109567763..109574384hg19UCSC Ensembl
Innerchr1:109369286..109375907hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg386622
hg196622
hg186622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547433
Supporting Variants
Samples
Known GenesWDR47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv721191
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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