A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946901



Internal ID18247065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148547900..148549123hg38UCSC Ensembl
Innerchr1:148273277..148274500hg19UCSC Ensembl
Innerchr1:146639901..146641124hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg381224
hg191224
hg181224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2594673, nssv2594676, nssv2594640, nssv2594636, nssv2594643, nssv2594670, nssv2594669, nssv2594675, nssv2594645, nssv2594637, nssv2594639, nssv2594644, nssv2594674, nssv2594638, nssv2594642, nssv2594678, nssv2594677, nssv2594671, nssv2594641, nssv2594672
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC101929780, NBPF10, NBPF14, NBPF8, NBPF9
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946901
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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