A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953375



Internal ID17302249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:1701129..1705128hg38UCSC Ensembl
Outerchr2:1704901..1708900hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001666
SamplesBILGI_BIOE
Known GenesPXDN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953375
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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