A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056625



Internal ID19145844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52876233..52940242hg38UCSC Ensembl
Innerchr17:50953593..51017602hg19UCSC Ensembl
Innerchr17:48308592..48372601hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3864010
hg1964010
hg1864010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568613
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)nsv1056625
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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