A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502753



Internal ID22560694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73375644..73402213hg38UCSC Ensembl
chr7:72789960..72816543hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3826570
hg1926584
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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