A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954649



Internal ID16956836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:9123158..9123339hg38UCSC Ensembl
Outerchr1:9183217..9183398hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000464
SamplesBILGI_BIOE
Known GenesGPR157
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954649
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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