A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758412



Internal ID16052368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106727422..107842134hg38UCSC Ensembl
Innerchr10:108487180..109601892hg19UCSC Ensembl
Innerchr10:108477170..109591882hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381114713
hg191114713
hg181114713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552158
Supporting Variants
Samples
Known GenesSORCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv758412
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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