A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981618



Internal ID18863043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:141486758..141487758hg38UCSC Ensembl
Outerchr3:141205600..141206600hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145004
Supporting Variants
SamplesKWS1
Known GenesRASA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981618
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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