A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510636



Internal ID18808917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24088733..24099347hg38UCSC Ensembl
Innerchr10:24377662..24388276hg19UCSC Ensembl
Innerchr10:24417668..24428282hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810615
hg1910615
hg1810615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045300
Supporting Variants
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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