A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952165



Internal ID17301039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:151458725..151459324hg38UCSC Ensembl
Outerchr1:151431201..151431800hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997320
SamplesBILGI_BIOE
Known GenesPOGZ
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952165
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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