A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114929



Internal ID18926111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:15455856..15475193hg38UCSC Ensembl
Outerchr1:15782351..15801688hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3819338
hg1919338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975224
SamplesKWS1
Known GenesCELA2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114929
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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