A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059856



Internal ID19149075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19596411..19639873hg38UCSC Ensembl
Innerchr17:19499724..19543186hg19UCSC Ensembl
Innerchr17:19440316..19483778hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3843463
hg1943463
hg1843463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3720015, nssv3560884
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)nsv1059856
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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