A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951213



Internal ID16953400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137824349..137845948hg38UCSC Ensembl
Outerchr9:140718801..140740400hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3821600
hg1921600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997049
SamplesBILGI_BIOE
Known GenesEHMT1, MIR602
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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