A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392169



Internal ID21383199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150261103..150261171hg38UCSC Ensembl
chr5:149640666..149640734hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703623
Samples
Known GenesCAMK2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392169
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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