A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950906



Internal ID16953093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96488719..96498018hg38UCSC Ensembl
Outerchr9:99251001..99260300hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996938
SamplesBILGI_BIOE
Known GenesHABP4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950906
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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