A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2536686



Internal ID17771350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65270665..65282593hg38UCSC Ensembl
Innerchr9:42719850..42731774hg19UCSC Ensembl
Innerchr9:42709846..42721770hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811929
hg1911925
hg1811925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972706
Supporting Variants
SamplesHGDP00542
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2536686
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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