A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446599



Internal ID22504469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119818790..120155724hg38UCSC Ensembl
chr7:119458844..119795778hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38336935
hg19336935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915311
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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