A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275734



Internal ID20842774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95499721..95500706hg38UCSC Ensembl
chr7:95129033..95130018hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559056
Supporting Variants
Samples
Known GenesASB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275734
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00066


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