A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951764



Internal ID16953951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126683322..126706421hg38UCSC Ensembl
Outerchr9:129445601..129468700hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3823100
hg1923100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996976
SamplesBILGI_BIOE
Known GenesLMX1B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951764
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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