A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328708



Internal ID20861857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6159926..6160541hg38UCSC Ensembl
chr1:6219986..6220601hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203644
Samples
Known GenesCHD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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