A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906436



Internal ID22681636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44103602..44103658hg38UCSC Ensembl
chr4:44105619..44105675hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906436
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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