A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705485



Internal ID21377761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124008815..124008878hg38UCSC Ensembl
chr12:124493362..124493425hg19UCSC 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 Variantsnsv4390494
Supporting Variants
Samples
Known GenesZNF664, ZNF664-FAM101A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705485
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0143678


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