A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999062



Internal ID16945328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:192808571..192819270hg38UCSC Ensembl
Outerchr1:192777701..192788400hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952595
Supporting Variants
SamplesBILGI_BIOE
Known GenesRGS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999062
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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