A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101759



Internal ID22010992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:82903556..82917167hg38UCSC Ensembl
chr2:83130680..83144291hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3813612
hg1913612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101759
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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