A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977386



Internal ID18265906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98861741..98867992hg38UCSC Ensembl
Innerchr13:99513995..99520246hg19UCSC Ensembl
Innerchr13:98311996..98318247hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg386252
hg196252
hg186252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762445
SamplesHGDP00998
Known GenesDOCK9
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977386
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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