A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044761



Internal ID19133980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62277804..62368374hg38UCSC Ensembl
Innerchr10:64037563..64128133hg19UCSC Ensembl
Innerchr10:63707569..63798139hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3890571
hg1990571
hg1890571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv879n100
Supporting Variantsnssv3511268
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)nsv1044761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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