A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064365



Internal ID18806896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20898426..20987403hg38UCSC Ensembl
Innerchr17:20801739..20890716hg19UCSC Ensembl
Innerchr17:20742331..20831308hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3888978
hg1988978
hg1888978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560924
Samples
Known GenesLOC440416
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064365
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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