A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999383



Internal ID16945649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33038203..33045002hg38UCSC Ensembl
Outerchr9:33038201..33045000hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950853
Supporting Variants
SamplesBILGI_BIOE
Known GenesDNAJA1, SMU1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999383
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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