A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273808



Internal ID20840848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15788827..16158399hg38UCSC Ensembl
chr7:15828452..16198024hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38369573
hg19369573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575520
Supporting Variants
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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