A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1007637



Internal ID16301593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137150461..137179201hg38UCSC Ensembl
Innerchr4:138071615..138100355hg19UCSC Ensembl
Innerchr4:138291065..138319805hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3828741
hg1928741
hg1828741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595523
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1007637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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