A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361691



Internal ID22587360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124008814..124008877hg38UCSC Ensembl
chr12:124493361..124493424hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947481
Supporting Variants
Samples
Known GenesZNF664, ZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361691
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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