A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758102



Internal ID19056383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6393886..6415025hg38UCSC Ensembl
Innerchr9:6393886..6415025hg19UCSC Ensembl
Innerchr9:6383886..6405025hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3821140
hg1921140
hg1821140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023419
Supporting Variants
Samples
Known GenesUHRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3758102
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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