A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275554



Internal ID20842594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32865301..34895818hg38UCSC Ensembl
chr7:32904913..34935430hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382030518
hg192030518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556652
Supporting Variants
Samples
Known GenesBBS9, BMPER, FKBP9, KBTBD2, NPSR1, NPSR1-AS1, NT5C3A, RP9, RP9P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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