A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275426



Internal ID20842466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5876114..7217703hg38UCSC Ensembl
chr7:5915745..7257334hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381341590
hg191341590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575349
Supporting Variants
Samples
Known GenesAIMP2, ANKRD61, C1GALT1, C7orf26, CCZ1, CCZ1B, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, LOC100131257, OCM, PMS2, PMS2CL, RAC1, RSPH10B, RSPH10B2, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275426
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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