A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256332



Internal ID21398888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5978874..6747083hg38UCSC Ensembl
chr7:6018505..6786714hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38768210
hg19768210
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730107
Supporting Variants
SamplesHG00731
Known GenesAIMP2, ANKRD61, C7orf26, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, PMS2, PMS2CL, RAC1, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256332
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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