A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174738



Internal ID15528183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133255089..133303529hg38UCSC Ensembl
Innerchr10:135068593..135117033hg19UCSC Ensembl
Innerchr10:134918584..134967023hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3848441
hg1948441
hg1848440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552587
Supporting Variants
SamplesHGDP00602
Known GenesADAM8, TUBGCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174738
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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