A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402216



Internal ID21059769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76868738..76873422hg38UCSC Ensembl
chr5:76164563..76169247hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg384685
hg194685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134503
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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