A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603763



Internal ID16044486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:75213889..75299710hg38UCSC Ensembl
Innerchr6:75923605..76009426hg19UCSC Ensembl
Innerchr6:75980325..76066146hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3885822
hg1985822
hg1885822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1064519
Samples
Known GenesCOX7A2, LOC100506804, TMEM30A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603763
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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