A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149564



Internal ID19198412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126531400..126531499hg38UCSC Ensembl
Outerchr3:126250243..126250342hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000865
SamplesKWB1
Known GenesCHST13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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