A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377046



Internal ID21034599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67710636..67712243hg38UCSC Ensembl
chr4:68576354..68577961hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381608
hg191608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119479
Samples
Known GenesUBA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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