A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975699



Internal ID18264220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46122042..46123595hg38UCSC Ensembl
Innerchr10:51472227..51473780hg19UCSC Ensembl
Innerchr10:51142233..51143786hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381554
hg191554
hg181554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2614122, nssv2614125, nssv2614121, nssv2614127, nssv2614123, nssv2614124, nssv2614126, nssv2614130, nssv2614129, nssv2614128
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAGAP7
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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