A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603505



Internal ID20976576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133810537..133949378hg38UCSC Ensembl
chr6:134131675..134270516hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38138842
hg19138842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215596
Samples
Known GenesMGC34034, TCF21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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