A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396444



Internal ID21053997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85579867..85597530hg38UCSC Ensembl
chr6:86289585..86307248hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3817664
hg1917664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220908
Samples
Known GenesSNX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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