A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327196



Internal ID20860333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173447294..173460136hg38UCSC Ensembl
chr1:173416433..173429275hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3812843
hg1912843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053121
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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