A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503386



Internal ID22561327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155209541..155215153hg38UCSC Ensembl
chr7:155001251..155006863hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg385613
hg195613
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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