A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1046176



Internal ID15899362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178917647..178925001hg38UCSC Ensembl
Innerchr5:178344648..178352002hg19UCSC Ensembl
Innerchr5:178277254..178284608hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387355
hg197355
hg187355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600465
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)nssv1046176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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