A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690122



Internal ID18988403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144910942..144941493hg38UCSC Ensembl
Innerchr8:146136327..146166879hg19UCSC Ensembl
Innerchr8:146107131..146137683hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3830552
hg1930553
hg1830553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027878
Supporting Variants
Samples
Known GenesZNF16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690122
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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