A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541715



Internal ID20914997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160177259..160178001hg38UCSC Ensembl
chr2:161033770..161034512hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n223
Supporting Variantsnssv18255382
Samples
Known GenesITGB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541715
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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