A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971762



Internal ID18260293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49990996..49992151hg38UCSC Ensembl
Innerchr10:51750756..51751911hg19UCSC Ensembl
Innerchr10:51420762..51421917hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381156
hg191156
hg181156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2613008, nssv2613014, nssv2613012, nssv2613011, nssv2613010, nssv2613006, nssv2613009, nssv2613015, nssv2613013, nssv2613007
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAGAP6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971762
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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