A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156895



Internal ID15533123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141423157..141457475hg38UCSC Ensembl
Innerchr8:142433257..142467575hg19UCSC Ensembl
Innerchr8:142502439..142536757hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3834319
hg1934319
hg1834319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612580
Supporting Variants
SamplesNINDS_111
Known GenesMROH5, PTP4A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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