A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543844



Internal ID20917085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38669784..38670029hg38UCSC Ensembl
chr2:38896926..38897171hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260203
Samples
Known GenesGALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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