A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537043



Internal ID20910382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62349499..62350247hg38UCSC Ensembl
chr2:62576634..62577382hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3904n223
Supporting Variantsnssv18260844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537043
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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