A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945861



Internal ID18592711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:29758484..29759091hg38UCSC Ensembl
Innerchr1:30231331..30231938hg19UCSC Ensembl
Innerchr1:30003918..30004525hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1757003, nssv1756996, nssv1756999, nssv1756998, nssv1756994, nssv1757000, nssv1757001, nssv1756997, nssv1756995, nssv1757002
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945861
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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