A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603810



Internal ID16391219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77568058..77651453hg38UCSC Ensembl
Innerchr6:78277775..78361170hg19UCSC Ensembl
Innerchr6:78334494..78417889hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3883396
hg1983396
hg1883396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1065568
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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