A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595585



Internal ID16382994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139313206..139317046hg38UCSC Ensembl
Innerchr4:140234360..140238200hg19UCSC Ensembl
Innerchr4:140453810..140457650hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg383841
hg193841
hg183841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9293n54
Supporting Variantsnssv1008214
Samples
Known GenesNAA15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595585
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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