A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433337



Internal ID22491207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29268490..29268541hg38UCSC Ensembl
chr7:29308106..29308157hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918419
Supporting Variants
Samples
Known GenesCHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433337
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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