A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387022



Internal ID21044575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121055496..121055648hg38UCSC Ensembl
chr4:121976651..121976803hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108947
Samples
Known GenesNDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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