A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047137



Internal ID19136356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8658738..8679800hg38UCSC Ensembl
Innerchr10:8700701..8721763hg19UCSC Ensembl
Innerchr10:8740707..8761769hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3821063
hg1921063
hg1821063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv669n100
Supporting Variantsnssv3500818
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)nsv1047137
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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