A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751857



Internal ID16045813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80453946..80454751hg38UCSC Ensembl
Innerchr10:82213702..82214507hg19UCSC Ensembl
Innerchr10:82203682..82204487hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551639
Supporting Variants
Samples
Known GenesTSPAN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751857
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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