A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134963



Internal ID19273351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150719003..150719299hg38UCSC Ensembl
Outerchr1:150691479..150691775hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv199n106
Supporting Variantsnssv3988502
SamplesKWS2
Known GenesHORMAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134963
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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