A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951196



Internal ID17300070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63259929..63331628hg38UCSC Ensembl
Outerchr9:67214901..67286600hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3871700
hg1971700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996848
SamplesBILGI_BIOE
Known GenesAQP7P1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951196
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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