A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435169



Internal ID21397171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155956307..155960306hg38UCSC Ensembl
chr7:155749001..155753000hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747115, nssv15749191
SamplesMDQ045, MDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435169
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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