A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275873



Internal ID20842913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99969003..99970314hg38UCSC Ensembl
chr7:99566626..99567937hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570306
Supporting Variants
Samples
Known GenesAZGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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