A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104868



Internal ID22014101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64297091..64410492hg38UCSC Ensembl
chr7:63757469..63870870hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38113402
hg19113402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573896
Samples
Known GenesZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104868
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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