A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996878



Internal ID16290834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44959516..45002970hg38UCSC Ensembl
Innerchr4:44961533..45004987hg19UCSC Ensembl
Innerchr4:44656290..44699744hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3843455
hg1943455
hg1843455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594100
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)nssv996878
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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