A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997128



Internal ID17290080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:39713329..39725028hg38UCSC Ensembl
Outerchr1:40179001..40190700hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950643
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997128
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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