A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561379



Internal ID20934450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88043302..88044815hg38UCSC Ensembl
chr7:87672617..87674130hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6998n223
Supporting Variantsnssv18276847
Samples
Known GenesADAM22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561379
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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