A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490252



Internal ID19077893
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 StatusS
Merged Variantsnsv1046720
Supporting Variants
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)nssv3490252
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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