A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604814



Internal ID16392223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143877672..143883473hg38UCSC Ensembl
Innerchr6:144198809..144204610hg19UCSC Ensembl
Innerchr6:144240502..144246303hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg385802
hg195802
hg185802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074240
Samples
Known GenesZC2HC1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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