A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594102



Internal ID16381511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44966586..45005191hg38UCSC Ensembl
Innerchr4:44968603..45007208hg19UCSC Ensembl
Innerchr4:44663360..44701965hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3838606
hg1938606
hg1838606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9030n54
Supporting Variantsnssv996901
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594102
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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