A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503420



Internal ID22561361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1582567..1585195hg38UCSC Ensembl
chr7:1622203..1624831hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382629
hg192629
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845894
Supporting Variants
Samples
Known GenesPSMG3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503420
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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