A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253964



Internal ID20821004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95114700..95114815hg38UCSC Ensembl
chr1:95580256..95580371hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545576
Supporting Variants
Samples
Known GenesTMEM56
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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