A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955108



Internal ID16957295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:24251462..24251567hg38UCSC Ensembl
Outerchr2:24474331..24474436hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003994
SamplesBILGI_BIOE
Known GenesITSN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955108
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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