A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503942



Internal ID22561885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131907354..131912067hg38UCSC Ensembl
chr7:131592113..131596826hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg384714
hg194714
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503942
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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