A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010579



Internal ID19099796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99941910..100182973hg38UCSC Ensembl
Innerchr3:99660754..99901817hg19UCSC Ensembl
Innerchr3:101143444..101384507hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38241064
hg19241064
hg18241064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4829n100
Supporting Variantsnssv3735189
Samples
Known GenesCMSS1, FILIP1L, MIR3921, MIR548G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010579
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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