A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970383



Internal ID19217113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:48412311..48412532hg38UCSC Ensembl
Outerchr4:48414328..48414549hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134044
Supporting Variants
SamplesKWS1
Known GenesSLAIN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970383
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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