A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275531



Internal ID20842571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32354819..33704107hg38UCSC Ensembl
chr7:32394431..33743719hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381349289
hg191349289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565335
Supporting Variants
Samples
Known GenesAVL9, BBS9, DPY19L1P1, FKBP9, KBTBD2, LINC00997, LOC100130673, LSM5, MIR550A2, MIR550B2, NT5C3A, RP9, RP9P, ZNRF2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275531
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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