A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2723446



Internal ID17493755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39118047..39119137hg38UCSC Ensembl
Innerchr9:39118044..39119134hg19UCSC Ensembl
Innerchr9:39108044..39109134hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982366
Supporting Variants
SamplesHGDP00998
Known GenesCNTNAP3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2723446
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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