A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945708



Internal ID18245873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:257667..266240hg38UCSC Ensembl
Innerchr1:227418..235991hg19UCSC Ensembl
Innerchr1:217161..225854hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg388574
hg198574
hg188694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2575119, nssv1752477, nssv1752521, nssv2575120, nssv2575113, nssv1753500, nssv2575114, nssv1752543, nssv2575117, nssv1752532, nssv1752554, nssv2575115, nssv1752488, nssv2575112, nssv1752510, nssv1752499, nssv1752565, nssv2575118, nssv2575111, nssv2575116
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945708
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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