A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575765



Internal ID16363174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58126424..58134484hg38UCSC Ensembl
Innerchr17:56203785..56211845hg19UCSC Ensembl
Innerchr17:53558784..53566844hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg388061
hg198061
hg188061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5727n54
Supporting Variantsnssv875525
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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