A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039568



Internal ID18782099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97041087..97108572hg38UCSC Ensembl
Innerchr10:98800844..98868329hg19UCSC Ensembl
Innerchr10:98790834..98858319hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3867486
hg1967486
hg1867486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv963n100
Supporting Variantsnssv3508555
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)nsv1039568
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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