A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381414



Internal ID22439284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61940349..61940443hg38UCSC Ensembl
chr16:61974253..61974347hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937295
Supporting Variants
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381414
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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