A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604446



Internal ID16391855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107114388..107115022hg38UCSC Ensembl
Innerchr6:107435592..107436226hg19UCSC Ensembl
Innerchr6:107542285..107542919hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38635
hg19635
hg18635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10896n54
Supporting Variantsnssv1071896
Samples
Known GenesBEND3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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