A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975067



Internal ID18263589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116076369..116079842hg38UCSC Ensembl
Innerchr10:117835880..117839353hg19UCSC Ensembl
Innerchr10:117825870..117829343hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383474
hg193474
hg183474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765048
SamplesHGDP00521
Known GenesGFRA1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975067
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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