A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447055



Internal ID22504925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54565370..54565420hg38UCSC Ensembl
chr7:54633063..54633113hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907806
Supporting Variants
Samples
Known GenesLOC285878, VSTM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447055
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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