A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996415



Internal ID19194441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24569262..24574370hg38UCSC Ensembl
Outerchr1:24895753..24900861hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385109
hg195109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147629
Supporting Variants
SamplesKWB1
Known GenesNCMAP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996415
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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