A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709925



Internal ID15657195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10624041..10781964hg38UCSC Ensembl
Innerchr1:10684098..10842021hg19UCSC Ensembl
Innerchr1:10606685..10764608hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38157924
hg19157924
hg18157924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545400
Supporting Variants
Samples
Known GenesCASZ1, PEX14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709925
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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