A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914854



Internal ID22690071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39778394..39780154hg38UCSC Ensembl
chr7:39817993..39819753hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381761
hg191761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440286
Samples
Known GenesLINC00265
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914854
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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