A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951747



Internal ID17300621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64347012..64452186hg38UCSC Ensembl
Outerchr9:43047501..43158300hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38105175
hg19110800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999436
SamplesBILGI_BIOE
Known GenesANKRD20A2, ANKRD20A3, LOC642929
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951747
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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