A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893755



Internal ID22668819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149938579..149954517hg38UCSC Ensembl
chr6:150259715..150275653hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3815939
hg1915939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414638
Samples
Known GenesULBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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