A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147176



Internal ID346358
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 StatusM
Merged Variantsdgv418n206
Supporting Variantsnssv16977978
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147176
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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