A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294808



Internal ID20504026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29264118..29264195hg38UCSC Ensembl
chr7:29303734..29303811hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738134
Supporting Variants
Samples
Known GenesCHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294808
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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