A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327218



Internal ID20860355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173920201..173921920hg38UCSC Ensembl
chr1:173889339..173891058hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381720
hg191720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327218
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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