A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323824



Internal ID20856946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21574586..21575115hg38UCSC Ensembl
chr1:21901079..21901608hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057969
Samples
Known GenesALPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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