A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711521



Internal ID16005477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24471893..24480524hg38UCSC Ensembl
Innerchr1:24798383..24807014hg19UCSC Ensembl
Innerchr1:24670970..24679601hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388632
hg198632
hg188632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545805
Supporting Variants
Samples
Known GenesNIPAL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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