A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2564624



Internal ID17870677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106977369..106979277hg38UCSC Ensembl
Innerchr9:109739650..109741558hg19UCSC Ensembl
Innerchr9:108779471..108781379hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381909
hg191909
hg181909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968743
Supporting Variants
SamplesHGDP01284
Known GenesMIR548Q, ZNF462
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)nssv2564624
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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