A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561748



Internal ID20934819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112208111..112208787hg38UCSC Ensembl
chr7:111848166..111848842hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273685
Samples
Known GenesZNF277
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561748
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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