A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445496



Internal ID22503366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104131789..104134351hg38UCSC Ensembl
chr7:103772236..103774798hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382563
hg192563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908747
Supporting Variants
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445496
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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