A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967243



Internal ID18602471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95978514..95995838hg38UCSC Ensembl
Innerchr3:95697358..95714682hg19UCSC Ensembl
Innerchr3:97180048..97197372hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3817325
hg1917325
hg1817325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758382
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967243
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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