A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057082



Internal ID19146301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6229127hg38UCSC Ensembl
Innerchr17:6106486..6132447hg19UCSC Ensembl
Innerchr17:6047210..6073171hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3825962
hg1925962
hg1825962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560150, nssv3560151, nssv3560149
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)nsv1057082
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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