A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104337



Internal ID22013571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76781759..76801673hg38UCSC Ensembl
chr2:77008885..77028799hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3819915
hg1919915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535820
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104337
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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