A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040262



Internal ID18782793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97045579..97112377hg38UCSC Ensembl
Innerchr10:98805336..98872134hg19UCSC Ensembl
Innerchr10:98795326..98862124hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3866799
hg1966799
hg1866799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv963n100
Supporting Variantsnssv3511893
Samples
Known GenesLOC100505540, SLIT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040262
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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