A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953444



Internal ID17302318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:9548772..9555571hg38UCSC Ensembl
Outerchr2:9688901..9695700hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001683
SamplesBILGI_BIOE
Known GenesADAM17
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953444
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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