A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956099



Internal ID17304972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128464670..128464843hg38UCSC Ensembl
Outerchr9:131226949..131227122hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002372
SamplesBILGI_BIOE
Known GenesODF2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956099
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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