A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054572



Internal ID18797103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89712199..89777313hg38UCSC Ensembl
Innerchr10:91471956..91537070hg19UCSC Ensembl
Innerchr10:91461936..91527050hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3865115
hg1965115
hg1865115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522675
Samples
Known GenesKIF20B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054572
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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