A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575847



Internal ID16363256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62940062..63174891hg38UCSC Ensembl
Innerchr17:61017423..61252252hg19UCSC Ensembl
Innerchr17:58371155..58605984hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38234830
hg19234830
hg18234830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5741n54
Supporting Variantsnssv875746
Samples
Known GenesMIR548W, TANC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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