A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399712



Internal ID22457582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76851082..76851082hg38UCSC Ensembl
chr18:74563038..74563038hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978360
Supporting Variants
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399712
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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