A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127895



Internal ID18936691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:37860884..37860937hg38UCSC Ensembl
Outerchr21:39233186..39233239hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956515
SamplesKWS1
Known GenesKCNJ6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127895
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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