A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395033



Internal ID21052586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76373093..76377332hg38UCSC Ensembl
chr4:77294246..77298485hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg384240
hg194240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120264
Samples
Known GenesCCDC158
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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