A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059445



Internal ID19148664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6229395hg38UCSC Ensembl
Innerchr17:6106486..6132715hg19UCSC Ensembl
Innerchr17:6047210..6073439hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3826230
hg1926230
hg1826230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560156, nssv3560154, nssv3560153, nssv3560152, nssv3560155
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)nsv1059445
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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