A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998431



Internal ID16944697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104493864..104816163hg38UCSC Ensembl
Outerchr14:104960201..105282500hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38322300
hg19322300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952271
Supporting Variants
SamplesBILGI_BIOE
Known GenesADSSL1, AKT1, C14orf180, INF2, MIR4710, SIVA1, TMEM179, ZBTB42
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998431
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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