A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392329



Internal ID21383359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36102343..36102416hg38UCSC Ensembl
chr6:36070120..36070193hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703757
Samples
Known GenesMAPK14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392329
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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