A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2541840



Internal ID17782471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61822142..61849212hg38UCSC Ensembl
Innerchr9:44958294..44985364hg19UCSC Ensembl
Innerchr9:44898188..44925360hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3827071
hg1927071
hg1827173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972721
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2541840
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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