A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048762



Internal ID19137981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29801935..29837823hg38UCSC Ensembl
Innerchr10:30090864..30126752hg19UCSC Ensembl
Innerchr10:30130870..30166758hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3835889
hg1935889
hg1835889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv700n100
Supporting Variantsnssv3707748, nssv3514159
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048762
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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