A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635909



Internal ID21827956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56689828..56689828hg38UCSC Ensembl
chr18:54357059..54357059hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110791
Supporting Variants
Samples
Known GenesWDR7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635909
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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