A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035405



Internal ID19124624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66158287..66330108hg38UCSC Ensembl
Innerchr10:67918045..68089866hg19UCSC Ensembl
Innerchr10:67588051..67759872hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38171822
hg19171822
hg18171822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv893n100
Supporting Variantsnssv3707929
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035405
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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