A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322534



Internal ID20855647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217351683..217413813hg38UCSC Ensembl
chr1:217525025..217587155hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3862131
hg1962131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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