A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361067



Internal ID21018620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6690768..6697288hg38UCSC Ensembl
chr4:6692495..6699015hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386521
hg196521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119428
Samples
Known GenesS100P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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