A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945878



Internal ID18592728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35350726..35353791hg38UCSC Ensembl
Innerchr1:35816327..35819392hg19UCSC Ensembl
Innerchr1:35588914..35591979hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383066
hg193066
hg183066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1759867, nssv1759873, nssv1759868, nssv1759866, nssv1759874, nssv1759872, nssv1759865, nssv1759869, nssv1759870, nssv1759871
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZMYM4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945878
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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