A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945846



Internal ID18592696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27164334..27211307hg38UCSC Ensembl
Innerchr1:27490825..27537798hg19UCSC Ensembl
Innerchr1:27363412..27410385hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3846974
hg1946974
hg1846974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1766479, nssv1766476, nssv1766477, nssv1766481, nssv1766474, nssv1766473, nssv1766478, nssv1766475, nssv1766472, nssv1766480
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)nsv945846
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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