A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393721



Internal ID21051274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155859824..155860525hg38UCSC Ensembl
chr4:156780976..156781677hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110269
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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