A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435025



Internal ID21397027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76838208..77074542hg38UCSC Ensembl
chr6:77547925..77784259hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38236335
hg19236335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748921
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435025
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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