A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325165



Internal ID20858295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24642001..24644100hg38UCSC Ensembl
chr1:24968492..24970591hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200701
Samples
Known GenesSRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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