A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591147



Internal ID16378556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99910043..99910723hg38UCSC Ensembl
Innerchr3:99628887..99629567hg19UCSC Ensembl
Innerchr3:101111577..101112257hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38681
hg19681
hg18681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv970673, nssv970675, nssv970671, nssv970670, nssv970676, nssv970677, nssv970672, nssv970674
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591147
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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