A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324180



Internal ID20857305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167087488..167087953hg38UCSC Ensembl
chr1:167056725..167057190hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053543
Samples
Known GenesGPA33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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