A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046720



Internal ID19135939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6644503..6790452hg38UCSC Ensembl
Innerchr10:6686465..6832414hg19UCSC Ensembl
Innerchr10:6726471..6872420hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38145950
hg19145950
hg18145950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv668n100
Supporting Variantsnssv3490252
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046720
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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