A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605492



Internal ID16392901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168686412..168725230hg38UCSC Ensembl
Innerchr6:169086528..169125339hg19UCSC Ensembl
Innerchr6:168828453..168867264hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3838819
hg1938812
hg1838812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155806
Samples1780854354_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605492
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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