A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607095



Internal ID21799142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53953525..53953623hg38UCSC Ensembl
chr14:54420243..54420341hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029579
Supporting Variants
Samples
Known GenesBMP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607095
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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