A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967068



Internal ID18602297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134434180..134446283hg38UCSC Ensembl
Innerchr3:134153022..134165125hg19UCSC Ensembl
Innerchr3:135635712..135647815hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3812104
hg1912104
hg1812104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2294996, nssv2294994, nssv2294989, nssv2294995, nssv2294991, nssv2294988, nssv2294993, nssv2294992, nssv2294990, nssv2294997
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR4788
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967068
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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