A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044977



Internal ID18787508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8506177..9072273hg38UCSC Ensembl
Innerchr10:8548140..9114236hg19UCSC Ensembl
Innerchr10:8588146..9154242hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38566097
hg19566097
hg18566097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494328
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044977
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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