A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253967



Internal ID20821007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95317719..95774568hg38UCSC Ensembl
chr1:95783275..96240124hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38456850
hg19456850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540631
Supporting Variants
Samples
Known GenesFLJ31662
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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