A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953949



Internal ID16956136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3959703..4089602hg38UCSC Ensembl
Outerchr19:3959701..4089600hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38129900
hg19129900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998928
SamplesBILGI_BIOE
Known GenesDAPK3, EEF2, MIR637, PIAS4, SNORD37, ZBTB7A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953949
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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