A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606986



Internal ID16394395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51731192..51768316hg38UCSC Ensembl
Innerchr7:51798888..51836012hg19UCSC Ensembl
Innerchr7:51766382..51803506hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3837125
hg1937125
hg1837125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1084576
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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