A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448464



Internal ID22506334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44213339..44213489hg38UCSC Ensembl
chr6:44181076..44181226hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448464
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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