A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503590



Internal ID22561531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:871491..880118hg38UCSC Ensembl
chr7:911128..919755hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg388628
hg198628
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847173
Supporting Variants
Samples
Known GenesGET4, SUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503590
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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