A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111771



Internal ID19258551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:66423117..66440117hg38UCSC Ensembl
Outerchr1:66888800..66905800hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3817001
hg1917001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv98n106
Supporting Variantsnssv3964680
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111771
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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