A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756035



Internal ID15703305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98193513..98227527hg38UCSC Ensembl
Innerchr10:99953270..99987284hg19UCSC Ensembl
Innerchr10:99943260..99977274hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3834015
hg1934015
hg1834015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552027
Supporting Variants
Samples
Known GenesR3HCC1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756035
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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