A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327458



Internal ID20860597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154498743..154499008hg38UCSC Ensembl
chr1:154471219..154471484hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052028
Samples
Known GenesSHE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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