A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563699



Internal ID20936770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63500717..63501096hg38UCSC Ensembl
chr6:64210622..64211001hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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