A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274402



Internal ID20841442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139070790..139071179hg38UCSC Ensembl
chr7:138755536..138755925hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563503
Supporting Variants
Samples
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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