A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945788



Internal ID18592638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15792862..15796022hg38UCSC Ensembl
Innerchr1:16119357..16122517hg19UCSC Ensembl
Innerchr1:15991944..15995104hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383161
hg193161
hg183161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1755649, nssv1755647, nssv1755646, nssv1755652, nssv1755651, nssv1755655, nssv1755654, nssv1755653, nssv1755648, nssv1755650
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945788
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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