A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145331



Internal ID18929564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31206048..31206106hg38UCSC Ensembl
Outerchr1:31678895..31678953hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982431
SamplesKWS1
Known GenesNKAIN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145331
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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