A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378749



Internal ID21036302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99277101..99278000hg38UCSC Ensembl
chr4:100198258..100199157hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121314
Samples
Known GenesADH1A, LOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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