A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326192



Internal ID20859326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61642601..61672400hg38UCSC Ensembl
chr1:62108273..62138072hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3829800
hg1929800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203647
Samples
Known GenesMGC34796
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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