A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334898



Internal ID20868087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:215353075..215380239hg38UCSC Ensembl
chr1:215526418..215553582hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3827165
hg1927165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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