A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604424



Internal ID16045147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104813190..104814546hg38UCSC Ensembl
Innerchr6:105261065..105262421hg19UCSC Ensembl
Innerchr6:105367758..105369114hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381357
hg191357
hg181357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10892n54
Supporting Variantsnssv1071849, nssv1071851, nssv1071852, nssv1071848, nssv1071847, nssv1071850
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604424
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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