A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986199



Internal ID19207846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:45726859..45727184hg38UCSC Ensembl
Outerchr3:45768351..45768676hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123642
Supporting Variants
SamplesKWS1
Known GenesSACM1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986199
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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