A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058269



Internal ID19147488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6229442hg38UCSC Ensembl
Innerchr17:6106486..6132762hg19UCSC Ensembl
Innerchr17:6047210..6073486hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3826277
hg1926277
hg1826277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560179, nssv3560187, nssv3560178, nssv3560170, nssv3560180, nssv3560193, nssv3560166, nssv3560168, nssv3560195, nssv3560173, nssv3560192, nssv3560162, nssv3560167, nssv3560194, nssv3560165, nssv3560169, nssv3560190, nssv3560163, nssv3560182, nssv3719156, nssv3560177, nssv3560174, nssv3560171, nssv3560164, nssv3560191, nssv3560159, nssv3560188, nssv3560185, nssv3560157, nssv3560183, nssv3560186, nssv3560161, nssv3560160, nssv3560181, nssv3560172, nssv3560189, nssv3560184, nssv3560175, nssv3560176, nssv3560158
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)nsv1058269
Frequency
Sample Size11257
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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