A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055042



Internal ID18797573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101363048..101571887hg38UCSC Ensembl
Innerchr10:103122805..103331644hg19UCSC Ensembl
Innerchr10:103112795..103321634hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38208840
hg19208840
hg18208840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv964n100
Supporting Variantsnssv3706208
Samples
Known GenesBTRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055042
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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