A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596372



Internal ID16383781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185299224..185347422hg38UCSC Ensembl
Innerchr4:186220378..186268576hg19UCSC Ensembl
Innerchr4:186457372..186505570hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3848199
hg1948199
hg1848199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017981
Samples
Known GenesSNX25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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