A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010793



Internal ID18753325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27214723..27282027hg38UCSC Ensembl
Innerchr1:27541214..27608518hg19UCSC Ensembl
Innerchr1:27413801..27481105hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3867305
hg1967305
hg1867305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3477431, nssv3475703
Samples
Known GenesWDTC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010793
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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