A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953248



Internal ID17302122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19737492..19757291hg38UCSC Ensembl
Outerchr19:19848301..19868100hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3819800
hg1919800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999784
SamplesBILGI_BIOE
Known GenesLINC00663
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953248
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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