A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418737



Internal ID22476607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266086..16266135hg38UCSC Ensembl
chr6:16266317..16266366hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903466
Supporting Variants
Samples
Known GenesGMPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418737
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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