A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392467



Internal ID21383497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73446429..73446753hg38UCSC Ensembl
chr6:74156152..74156476hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703832
Samples
Known GenesMB21D1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392467
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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