A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945758



Internal ID18592609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8614398..8616370hg38UCSC Ensembl
Innerchr1:8674457..8676429hg19UCSC Ensembl
Innerchr1:8597044..8599016hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381973
hg191973
hg181973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1752574, nssv1752576, nssv1752577, nssv1752578, nssv1752579, nssv1752580, nssv1752582, nssv1752583, nssv1752581, nssv1752575
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRERE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945758
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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