A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325965



Internal ID20859099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23808981..23884089hg38UCSC Ensembl
chr1:24135471..24210579hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3875109
hg1975109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059270
Samples
Known GenesCNR2, FUCA1, HMGCL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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