A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2738395



Internal ID17840639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62884949..62931304hg38UCSC Ensembl
Innerchr9:66540773..66587128hg19UCSC Ensembl
Innerchr9:66280593..66326948hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3846356
hg1946356
hg1846356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972737
Supporting Variants
SamplesHGDP00998
Known GenesMGC21881
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2738395
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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