A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605594



Internal ID16393003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..176270hg38UCSC Ensembl
Innerchr7:45653..176270hg19UCSC Ensembl
Innerchr7:140736..271353hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38130618
hg19130618
hg18130618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155839
SamplesHGDP00183
Known GenesLOC100507642
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605594
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer