A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502768



Internal ID22560709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73818252..73820403hg38UCSC Ensembl
chr7:73232582..73234733hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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