A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273813



Internal ID20840853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158614485..158932639hg38UCSC Ensembl
chr7:158407177..158725330hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38318155
hg19318154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563680
Supporting Variants
Samples
Known GenesESYT2, NCAPG2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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