A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814151



Internal ID21259489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44390908..44390971hg38UCSC Ensembl
chr6:44358645..44358708hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702157
Samples
Known GenesCDC5L
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814151
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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