A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1046271



Internal ID15899457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178921604..178925244hg38UCSC Ensembl
Innerchr5:178348605..178352245hg19UCSC Ensembl
Innerchr5:178281211..178284851hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg383641
hg193641
hg183641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600476
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)nssv1046271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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