A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868149



Internal ID22643084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65150019..65150070hg38UCSC Ensembl
chr1:65615702..65615753hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389519
Samples
Known GenesAK4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868149
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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