A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429926



Internal ID22487796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42770662..42770927hg38UCSC Ensembl
chr6:42738400..42738665hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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