A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111625



Internal ID22020858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76851082..76851082hg38UCSC Ensembl
chr18:74563038..74563038hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635242
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111625
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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