A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055189



Internal ID19144408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52485035..52781102hg38UCSC Ensembl
Innerchr17:50562395..50858462hg19UCSC Ensembl
Innerchr17:47917394..48213461hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38296068
hg19296068
hg18296068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568611
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)nsv1055189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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