A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329837



Internal ID20862990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44188878..44191664hg38UCSC Ensembl
chr1:44654550..44657336hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382787
hg192787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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