A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287179



Internal ID20496397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9277706..9277817hg38UCSC Ensembl
chr18:9277704..9277815hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732467
Supporting Variants
Samples
Known GenesANKRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287179
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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