A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427864



Internal ID22485734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151390151..151390217hg38UCSC Ensembl
chr6:151711286..151711352hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905974
Supporting Variants
Samples
Known GenesZBTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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