A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951179



Internal ID16953366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39150973..39304033hg38UCSC Ensembl
Outerchr9:65561001..65584700hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38153061
hg1923700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996831
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951179
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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