A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758233



Internal ID18709828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14754012..14800261hg38UCSC Ensembl
Innerchr9:14754010..14800259hg19UCSC Ensembl
Innerchr9:14744010..14790259hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3846250
hg1946250
hg1846250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023955
Supporting Variants
Samples
Known GenesFREM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3758233
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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