A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150247



Internal ID19202796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:36740562..36740694hg38UCSC Ensembl
Outerchr1:37206163..37206295hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003546
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150247
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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