A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978907



Internal ID18267424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35496175..35502181hg38UCSC Ensembl
Innerchr19:35987077..35993083hg19UCSC Ensembl
Innerchr19:40678917..40684923hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386007
hg196007
hg186007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764477
SamplesHGDP00521
Known GenesDMKN
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978907
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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