A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424753



Internal ID21082306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138802276..138803819hg38UCSC Ensembl
chr7:138487021..138488564hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381544
hg191544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226894
Samples
Known GenesTMEM213
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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