A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121607



Internal ID19276592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:63270899..63271002hg38UCSC Ensembl
Outerchr3:63256575..63256678hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965614
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121607
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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