A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038178



Internal ID19127397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24083828..24099347hg38UCSC Ensembl
Innerchr10:24372757..24388276hg19UCSC Ensembl
Innerchr10:24412763..24428282hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3815520
hg1915520
hg1815520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv689n100
Supporting Variantsnssv3508300
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)nsv1038178
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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