A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998436



Internal ID16944702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104922864..105021963hg38UCSC Ensembl
Outerchr14:105389201..105488300hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3899100
hg1999100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952276
Supporting Variants
SamplesBILGI_BIOE
Known GenesAHNAK2, C14orf79, CDCA4, PLD4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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