A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036587



Internal ID19125806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55201700..55595907hg38UCSC Ensembl
Innerchr10:56961460..57355667hg19UCSC Ensembl
Innerchr10:56631466..57025673hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38394208
hg19394208
hg18394208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503101
Samples
Known GenesRNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036587
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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