A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602105



Internal ID16042828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32183666..32210123hg38UCSC Ensembl
Innerchr6:32151443..32177900hg19UCSC Ensembl
Innerchr6:32259421..32285878hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826458
hg1926458
hg1826458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154077
Samples1798860372_A
Known GenesAGER, GPSM3, NOTCH4, PBX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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