A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557901



Internal ID20930972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3003274..3052507hg38UCSC Ensembl
chr6:3003508..3052741hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3849234
hg1949234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6046n223
Supporting Variantsnssv18270534
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557901
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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