A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294393



Internal ID20503611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36343398..36343452hg38UCSC Ensembl
chr7:36383007..36383061hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731451
Supporting Variants
Samples
Known GenesKIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294393
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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