A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559660



Internal ID20932731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6467608..6468491hg38UCSC Ensembl
chr7:6507239..6508122hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274180
Samples
Known GenesKDELR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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