A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325823



Internal ID20858955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100678969..100710454hg38UCSC Ensembl
chr1:101144525..101176010hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3831486
hg1931486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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