A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557976



Internal ID20931047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1675075..1675745hg38UCSC Ensembl
chr6:1675309..1675979hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269960
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557976
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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