A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573324



Internal ID20946395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73472552..73473731hg38UCSC Ensembl
chr7:72886882..72888061hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276485
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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