A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604127



Internal ID16391536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90295555..90297030hg38UCSC Ensembl
Innerchr6:91005274..91006749hg19UCSC Ensembl
Innerchr6:91061995..91063470hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381476
hg191476
hg181476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1068394
Samples
Known GenesBACH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604127
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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