A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947786



Internal ID18594633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27246212..27252983hg38UCSC Ensembl
Innerchr10:27535141..27541912hg19UCSC Ensembl
Innerchr10:27575147..27581918hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386772
hg196772
hg186772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1836608, nssv1836615, nssv1836609, nssv1836613, nssv1836617, nssv1836612, nssv1836610, nssv1836611, nssv1836614, nssv1836616
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLRRC37A6P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947786
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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