A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951734



Internal ID17300608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40322683..40345182hg38UCSC Ensembl
Outerchr9:42467701..42490200hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3822500
hg1922500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999423
SamplesBILGI_BIOE
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951734
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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