A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951392



Internal ID16953579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109680179..109699578hg38UCSC Ensembl
Outerchr1:110222801..110242200hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819400
hg1919400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997196
SamplesBILGI_BIOE
Known GenesGSTM1, GSTM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951392
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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