A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445808



Internal ID22503678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82542117..82544251hg38UCSC Ensembl
chr7:82171433..82173567hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382135
hg192135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909734
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445808
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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