A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377916



Internal ID21035469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147529384..147530198hg38UCSC Ensembl
chr4:148450536..148451350hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109595
Samples
Known GenesEDNRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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