A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038739



Internal ID19127958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119303687..119336147hg38UCSC Ensembl
Innerchr10:121063199..121095659hg19UCSC Ensembl
Innerchr10:121053189..121085649hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3832461
hg1932461
hg1832461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510383
Samples
Known GenesGRK5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038739
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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