A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999332



Internal ID19158868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99971363..100055876hg38UCSC Ensembl
Innerchr3:99690207..99774720hg19UCSC Ensembl
Innerchr3:101172897..101257410hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3884514
hg1984514
hg1884514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604232
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999332
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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