A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751932



Internal ID16045888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81374678..82080786hg38UCSC Ensembl
Innerchr10:83134434..83840542hg19UCSC Ensembl
Innerchr10:83124414..83830522hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38706109
hg19706109
hg18706109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551669
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751932
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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