A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977978



Internal ID52722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3003320..3052546hg38UCSC Ensembl
chr6:3003554..3052780hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3849227
hg1949227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147176
Supporting Variants
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977978
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.025297


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