A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065720



Internal ID19154939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:239022..264687hg38UCSC Ensembl
Innerchr17:88813..114478hg19UCSC Ensembl
Innerchr17:88813..114478hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3825666
hg1925666
hg1825666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560035
Samples
Known GenesRPH3AL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065720
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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