A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949445



Internal ID21369516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44390906..44390970hg38UCSC Ensembl
chr6:44358643..44358707hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197292
SamplesHG002
Known GenesCDC5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949445
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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