A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385034



Internal ID21042587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64976804..64977666hg38UCSC Ensembl
chr4:65842522..65843384hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118229
Samples
Known GenesLOC401134
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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