A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542533



Internal ID20915792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20715209..20790995hg38UCSC Ensembl
chr1:21041702..21117488hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3875787
hg1975787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250013
Samples
Known GenesHP1BP3, KIF17, SH2D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542533
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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