A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319590



Internal ID20852685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43629617..43641773hg38UCSC Ensembl
chr1:44095288..44107444hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3812157
hg1912157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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