A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565124



Internal ID20938195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5825535..7068762hg38UCSC Ensembl
chr7:5865166..7108393hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381243228
hg191243228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6551n223
Supporting Variantsnssv18275422
Samples
Known GenesAIMP2, ANKRD61, C7orf26, CCZ1, CCZ1B, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, OCM, PMS2, PMS2CL, RAC1, RSPH10B, RSPH10B2, USP42, ZDHHC4, ZNF12, ZNF316, ZNF815P, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565124
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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