A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434596



Internal ID21396598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180948135..181003755hg38UCSC Ensembl
chr5:180375135..180430755hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3855621
hg1955621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv670n172
Supporting Variantsnssv15746034
SamplesNB09
Known GenesBTNL3, BTNL8
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434596
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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