A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766181



Internal ID18964891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1029967..1030130hg38UCSC Ensembl
chr1:965347..965510hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073573
Supporting Variants
SamplesKWP1
Known GenesAGRN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766181
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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