A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998396



Internal ID16944662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:99504664..99604963hg38UCSC Ensembl
Outerchr14:99971001..100071300hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38100300
hg19100300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952236
Supporting Variants
SamplesBILGI_BIOE
Known GenesCCDC85C, CCNK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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