A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2742863



Internal ID17729865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64407350..64409983hg38UCSC Ensembl
Innerchr9:69419768..69422401hg19UCSC Ensembl
Innerchr9:68709588..68712221hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382634
hg192634
hg182634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969671
Supporting Variants
SamplesHGDP00456
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2742863
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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