A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110732



Internal ID19265158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:3199668..3199738hg38UCSC Ensembl
Outerchr2:3203439..3203509hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1846n106
Supporting Variantsnssv3961141
SamplesKWS1
Known GenesTSSC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110732
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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