A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050096



Internal ID19139315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62274914..62368374hg38UCSC Ensembl
Innerchr10:64034673..64128133hg19UCSC Ensembl
Innerchr10:63704679..63798139hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3893461
hg1993461
hg1893461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv879n100
Supporting Variantsnssv3707148, nssv3707147
Samples
Known GenesLOC283045
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050096
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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