A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325883



Internal ID20859016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167655095..167655616hg38UCSC Ensembl
chr1:167624332..167624853hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053563
Samples
Known GenesRCSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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