A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552049



Internal ID20925179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215385470..215386060hg38UCSC Ensembl
chr2:216250193..216250783hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258682
Samples
Known GenesFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552049
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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