A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504792



Internal ID22562736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24727973..24731172hg38UCSC Ensembl
chr7:24767592..24770791hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846275
Supporting Variants
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504792
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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