A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565117



Internal ID20938188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77704701..77705676hg38UCSC Ensembl
chr7:77334018..77334993hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276635
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565117
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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