A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547673



Internal ID20920874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135628730..135629114hg38UCSC Ensembl
chr2:136386300..136386684hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4132n223
Supporting Variantsnssv18255893
Samples
Known GenesR3HDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547673
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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