A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502630



Internal ID22560571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149499596..149509763hg38UCSC Ensembl
chr7:149196687..149206854hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3810168
hg1910168
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502630
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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