A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573908



Internal ID21765951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44390942..44391003hg38UCSC Ensembl
chr6:44358679..44358740hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003907
Supporting Variants
Samples
Known GenesCDC5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573908
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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