A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319891



Internal ID20852988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33798501..33803300hg38UCSC Ensembl
chr1:34264102..34268901hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060982
Samples
Known GenesCSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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