A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147629



Internal ID19200308
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 StatusM
Merged Variants
Supporting Variantsnssv3996415
SamplesKWB1
Known GenesNCMAP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147629
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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