A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2541133



Internal ID17773294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61615989..61673158hg38UCSC Ensembl
Innerchr9:44823827..44880996hg19UCSC Ensembl
Innerchr9:44763823..44820992hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3857170
hg1957170
hg1857170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972719
Supporting Variants
SamplesHGDP00542
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)nssv2541133
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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