A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360514



Internal ID22586183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124258735..124258891hg38UCSC Ensembl
chr12:124743281..124743437hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928496
Supporting Variants
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360514
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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