A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536177



Internal ID20909532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197189269..197190190hg38UCSC Ensembl
chr1:197158399..197159320hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38922
hg19922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248187
Samples
Known GenesZBTB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536177
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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