A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998375



Internal ID16944641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:77132858..77142257hg38UCSC Ensembl
Outerchr14:77599201..77608600hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952870
Supporting Variants
SamplesBILGI_BIOE
Known GenesZDHHC22
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998375
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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