A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2759055



Internal ID17831784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25754993..25760641hg38UCSC Ensembl
Innerchr1:26081484..26087132hg19UCSC Ensembl
Innerchr1:25954071..25959719hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385649
hg195649
hg185649
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947417
Supporting Variants
SamplesHGDP00998
Known GenesMAN1C1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2759055
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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