A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv873571



Internal ID16167527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53755645..53780149hg38UCSC Ensembl
Innerchr17:51833006..51857510hg19UCSC Ensembl
Innerchr17:49188005..49212509hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3824505
hg1924505
hg1824505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575588
Supporting Variants
Samples
Known GenesMIR548AJ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv873571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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