A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952830



Internal ID16955017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:38207696..38211495hg38UCSC Ensembl
Outerchr14:38676901..38680700hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998330
SamplesBILGI_BIOE
Known GenesSSTR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952830
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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