A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605820



Internal ID16046543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1518331..1574625hg38UCSC Ensembl
Innerchr7:1557967..1614261hg19UCSC Ensembl
Innerchr7:1524493..1580787hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3856295
hg1956295
hg1856295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078359
Samples
Known GenesMAFK, PSMG3, PSMG3-AS1, TMEM184A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605820
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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