A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606426



Internal ID16047149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25214506..25581959hg38UCSC Ensembl
Innerchr7:25254125..25621579hg19UCSC Ensembl
Innerchr7:25220650..25588104hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38367454
hg19367455
hg18367455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081140
Samples
Known GenesNPVF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606426
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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