A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756254



Internal ID16050210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106190953..106191690hg38UCSC Ensembl
Innerchr10:107950711..107951448hg19UCSC Ensembl
Innerchr10:107940701..107941438hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38738
hg19738
hg18738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756254
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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