A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945749



Internal ID18245914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1751857..1760427hg38UCSC Ensembl
Innerchr1:1683296..1691866hg19UCSC Ensembl
Innerchr1:1673156..1681726hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg388571
hg198571
hg188571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1750185, nssv1750181, nssv1750187, nssv1750183, nssv1750186, nssv1750180, nssv1750184, nssv1750182, nssv1750179, nssv1750178
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNADK
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945749
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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