A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954845



Internal ID16957032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16215106..16237105hg38UCSC Ensembl
Outerchr1:16541601..16563600hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3822000
hg1922000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003131
SamplesBILGI_BIOE
Known GenesRSG1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954845
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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