A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752137



Internal ID15699407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83260366..84632635hg38UCSC Ensembl
Innerchr10:85020122..86392391hg19UCSC Ensembl
Innerchr10:85010102..86382371hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381372270
hg191372270
hg181372270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551745
Supporting Variants
Samples
Known GenesC10orf99, CCSER2, CDHR1, GHITM, LINC00858, LRIT1, LRIT2, RGR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752137
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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