A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325195



Internal ID20858326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151318001..151321800hg38UCSC Ensembl
chr1:151290477..151294276hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051322
Samples
Known GenesPI4KB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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