A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953279



Internal ID16955466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34367296..34396295hg38UCSC Ensembl
Outerchr19:34858201..34887200hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3829000
hg1929000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999815
SamplesBILGI_BIOE
Known GenesGPI
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953279
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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