A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598315



Internal ID16385724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61331130..61333284hg38UCSC Ensembl
Innerchr5:60626957..60629111hg19UCSC Ensembl
Innerchr5:60662714..60664868hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382155
hg192155
hg182155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1034195
Samples
Known GenesZSWIM6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598315
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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