A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600447



Internal ID20973518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132766392..132781641hg38UCSC Ensembl
chr6:133087531..133102780hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3815250
hg1915250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215586
Samples
Known GenesSLC18B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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