A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251080



Internal ID20818120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37863235..37864001hg38UCSC Ensembl
chr1:38328907..38329673hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543693
Supporting Variants
Samples
Known GenesINPP5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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