A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504793



Internal ID22562737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24728573..24729572hg38UCSC Ensembl
chr7:24768192..24769191hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846900
Supporting Variants
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504793
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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