A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903739



Internal ID22678908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36988838..36988890hg38UCSC Ensembl
chr4:36990460..36990512hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903739
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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