A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005441



Internal ID17298393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:67329770..67329925hg38UCSC Ensembl
Outerchr14:67796487..67796642hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958770
Supporting Variants
SamplesBILGI_BIOE
Known GenesMPP5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005441
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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