A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508555



Internal ID18460150
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 StatusS
Merged Variantsnsv1039568
Supporting Variants
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)nssv3508555
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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