A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945527



Internal ID18592378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:409872..421456hg38UCSC Ensembl
Innerchr1:397881..409465hg19UCSC Ensembl
Innerchr1:387744..399328hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3811585
hg1911585
hg1811585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2571507, nssv2571506, nssv2571512, nssv2571508, nssv2571510, nssv2571505, nssv2571514, nssv2571513, nssv2571509, nssv2571511
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945527
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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