A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545714



Internal ID15986437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18250219..18305874hg38UCSC Ensembl
Innerchr1:18576713..18632368hg19UCSC Ensembl
Innerchr1:18449300..18504955hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3855656
hg1955656
hg1855656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711243
Samples
Known GenesIGSF21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545714
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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