A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005400



Internal ID17298352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:100378676..100379032hg38UCSC Ensembl
Outerchr14:100845013..100845369hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958726
Supporting Variants
SamplesBILGI_BIOE
Known GenesWDR25
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005400
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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