A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322893



Internal ID20856008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180851424..180852014hg38UCSC Ensembl
chr1:180820560..180821150hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054606
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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