A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1046280



Internal ID15899466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178921932..178925244hg38UCSC Ensembl
Innerchr5:178348933..178352245hg19UCSC Ensembl
Innerchr5:178281539..178284851hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg383313
hg193313
hg183313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600478
Supporting Variants
Samples
Known GenesZFP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1046280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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