A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573813



Internal ID20946884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107937632..107942595hg38UCSC Ensembl
chr7:107578077..107583040hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384964
hg194964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273605
Samples
Known GenesLAMB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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