A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036581



Internal ID19125800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89766948..89931779hg38UCSC Ensembl
Innerchr10:91526705..91691536hg19UCSC Ensembl
Innerchr10:91516685..91681516hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38164832
hg19164832
hg18164832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706188
Samples
Known GenesKIF20B, LINC00865
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036581
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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