A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955083



Internal ID16957270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:45415107..45415341hg38UCSC Ensembl
Outerchr2:45642246..45642480hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003907
SamplesBILGI_BIOE
Known GenesSRBD1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955083
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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