A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131735



Internal ID19259843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:149079463..149079517hg38UCSC Ensembl
Outerchr3:148797250..148797304hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986261
SamplesKWS1
Known GenesHLTF
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131735
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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