A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387869



Internal ID22445739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87755816..87773264hg38UCSC Ensembl
chr16:87789422..87806870hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3817449
hg1917449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936063
Supporting Variants
Samples
Known GenesKLHDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387869
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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