A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389530



Internal ID21047083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145801637..145802018hg38UCSC Ensembl
chr4:146722789..146723170hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108902
Samples
Known GenesZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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