A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961170



Internal ID19222456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:41378221..41378321hg38UCSC Ensembl
Outerchr21:42750148..42750248hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110761
Supporting Variants
SamplesKWS1
Known GenesMX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961170
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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