A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328268



Internal ID20861414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42856829..42859446hg38UCSC Ensembl
chr1:43322500..43325117hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382618
hg192618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060505
Samples
Known GenesLOC339539
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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