A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431365



Internal ID22489235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37653835..37665531hg38UCSC Ensembl
chr7:37693438..37705134hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3811697
hg1911697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431365
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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