A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603755



Internal ID16391164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74122829..74126569hg38UCSC Ensembl
Innerchr6:74832545..74836285hg19UCSC Ensembl
Innerchr6:74889265..74893005hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383741
hg193741
hg183741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10780n54
Supporting Variantsnssv1064495
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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