A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555551



Internal ID20928637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99146004..99146935hg38UCSC Ensembl
chr2:99762467..99763398hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261693
Samples
Known GenesC2orf15, TSGA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555551
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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