A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252431



Internal ID20819471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38994117..38994498hg38UCSC Ensembl
chr1:39459789..39460170hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545088
Supporting Variants
Samples
Known GenesAKIRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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