A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542131



Internal ID20915397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9513317..9513367hg38UCSC Ensembl
chr2:9653446..9653496hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261628
Samples
Known GenesADAM17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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