A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257467



Internal ID21400112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5841688..6817166hg38UCSC Ensembl
chr7:5881319..6856797hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38975479
hg19975479
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730107
Supporting Variants
SamplesNA19238
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
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257467
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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