A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250451



Internal ID20817491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6084606..6255340hg38UCSC Ensembl
chr1:6144666..6315400hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38170735
hg19170735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536999
Supporting Variants
Samples
Known GenesCHD5, GPR153, HES3, ICMT, KCNAB2, LINC00337, RNF207, RPL22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250451
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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