A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327779



Internal ID20860921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212913212..212915577hg38UCSC Ensembl
chr1:213086554..213088919hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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