A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536338



Internal ID21860693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25377645..25404500hg38UCSC Ensembl
chr1:25704136..25730991hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3826856
hg1926856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111750
Supporting Variants
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536338
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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