A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437664



Internal ID22495534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1582720..1583916hg38UCSC Ensembl
chr7:1622356..1623552hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918976
Supporting Variants
Samples
Known GenesPSMG3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437664
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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