A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575849



Internal ID16363258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62978029..63126903hg38UCSC Ensembl
Innerchr17:61055390..61204264hg19UCSC Ensembl
Innerchr17:58409122..58557996hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38148875
hg19148875
hg18148875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5742n54
Supporting Variantsnssv875747
Samples
Known GenesMIR548W, TANC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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