A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975866



Internal ID18870226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1029667..1029982hg38UCSC Ensembl
Outerchr1:965047..965362hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137176
Supporting Variants
SamplesKWS1
Known GenesAGRN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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