A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960409



Internal ID18595660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10527782..10530541hg38UCSC Ensembl
Innerchr17:10431099..10433858hg19UCSC Ensembl
Innerchr17:10371824..10374583hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382760
hg192760
hg182760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2076653, nssv2076647, nssv2076650, nssv2076651, nssv2076655, nssv2076656, nssv2076648, nssv2076649, nssv2076652, nssv2076654
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMYH2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960409
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer