A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998405



Internal ID17291357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101219864..101230263hg38UCSC Ensembl
Outerchr14:101686201..101696600hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952245
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998405
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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