A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156660



Internal ID15879810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143486205..143533025hg38UCSC Ensembl
Innerchr8:144568375..144615195hg19UCSC Ensembl
Innerchr8:144639518..144686338hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3846821
hg1946821
hg1846821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612772
Supporting Variants
SamplesNINDS_111
Known GenesZC3H3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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