A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055819



Internal ID19145038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56078491..56095230hg38UCSC Ensembl
Innerchr17:54155852..54172591hg19UCSC Ensembl
Innerchr17:51510851..51527590hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3816740
hg1916740
hg1816740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3267n100
Supporting Variantsnssv3566111, nssv3566110, nssv3566113, nssv3566112
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)nsv1055819
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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