A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326437



Internal ID20859572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36191901..36210400hg38UCSC Ensembl
chr1:36657502..36676001hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3818500
hg1918500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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