A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051779



Internal ID19140998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91075976..91113184hg38UCSC Ensembl
Innerchr10:92835733..92872941hg19UCSC Ensembl
Innerchr10:92825713..92862921hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3837209
hg1937209
hg1837209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521737
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)nsv1051779
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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