A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979888



Internal ID18268403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149981833..149984846hg38UCSC Ensembl
Innerchr3:149699620..149702633hg19UCSC Ensembl
Innerchr3:151182310..151185323hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg383014
hg193014
hg183014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2298384, nssv2298388, nssv2298385, nssv2298390, nssv2298391, nssv2298389, nssv2298387, nssv2298383, nssv2298386, nssv2298382
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979888
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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