A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595520



Internal ID16382929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:136840332..136893149hg38UCSC Ensembl
Innerchr4:137761486..137814303hg19UCSC Ensembl
Innerchr4:137980936..138033753hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3852818
hg1952818
hg1852818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153512
Samples1780862227_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595520
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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