A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995125



Internal ID19220407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:38861302..38861352hg38UCSC Ensembl
Outerchr1:39326974..39327024hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144369
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3995125
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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