A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv970377



Internal ID16264333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99909978..99910601hg38UCSC Ensembl
Innerchr3:99628822..99629445hg19UCSC Ensembl
Innerchr3:101111512..101112135hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38624
hg19624
hg18624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591145
Supporting Variants
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)nssv970377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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