A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945813



Internal ID18592663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21440874..21486086hg38UCSC Ensembl
Innerchr1:21767367..21812579hg19UCSC Ensembl
Innerchr1:21639954..21685166hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3845213
hg1945213
hg1845213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1763438, nssv1763431, nssv1763436, nssv1763432, nssv1763433, nssv1763434, nssv1763437, nssv1763439, nssv1763435, nssv1763440
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNBPF3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945813
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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