A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104808



Internal ID21289884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16597790..16875287hg38UCSC Ensembl
Innerchr1:16924285..17201782hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38277498
hg19277498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114785
Supporting Variants
Samplessample52
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104808
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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