A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005417



Internal ID17298369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:81130716..81131007hg38UCSC Ensembl
Outerchr14:81597060..81597351hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958743
Supporting Variants
SamplesBILGI_BIOE
Known GenesTSHR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005417
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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