A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954903



Internal ID17303776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:21868108..21938307hg38UCSC Ensembl
Outerchr1:22194601..22264800hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3870200
hg1970200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003152
SamplesBILGI_BIOE
Known GenesHSPG2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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