A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565335



Internal ID20938406
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 StatusM
Merged Variants
Supporting Variantsnssv18275531
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)nsv6565335
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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