A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333668



Internal ID20866848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155768665..155769585hg38UCSC Ensembl
chr1:155738456..155739376hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052092
Samples
Known GenesGON4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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