A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975224



Internal ID18878007
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 StatusS
Merged Variantsnsv1114929
Supporting Variants
SamplesKWS1
Known GenesCELA2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975224
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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