A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561925



Internal ID20934996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134883837..134885008hg38UCSC Ensembl
chr7:134568588..134569759hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7124n223
Supporting Variantsnssv18272587
Samples
Known GenesCALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561925
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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