A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918219



Internal ID22693440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16197548..16198816hg38UCSC Ensembl
chr7:16237173..16238441hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440341
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918219
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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