A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258566



Internal ID21399989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5860165..6820915hg38UCSC Ensembl
chr7:5899796..6860546hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38960751
hg19960751
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, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258566
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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