A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945838



Internal ID18246002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25887321..25891977hg38UCSC Ensembl
Innerchr1:26213812..26218468hg19UCSC Ensembl
Innerchr1:26086399..26091055hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384657
hg194657
hg184657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1766709, nssv1766705, nssv1766712, nssv1766708, nssv1766703, nssv1766710, nssv1766704, nssv1766711, nssv1766707, nssv1766706
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSTMN1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945838
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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