A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320608



Internal ID20853707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90955836..90978341hg38UCSC Ensembl
chr1:91421393..91443898hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3822506
hg1922506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203151
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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