A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551778



Internal ID16339187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86366288..86367652hg38UCSC Ensembl
Innerchr10:88126045..88127409hg19UCSC Ensembl
Innerchr10:88116025..88117389hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381365
hg191365
hg181365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1318n54
Supporting Variantsnssv752220, nssv752219
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551778
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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