A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509438



Internal ID22567388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93697836..93702989hg38UCSC Ensembl
chr7:93327148..93332301hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385154
hg195154
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509438
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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