A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982291



Internal ID19211084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:144140597..144158797hg38UCSC Ensembl
Outerchr8:145195500..145213700hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3818201
hg1918201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145205
Supporting Variants
SamplesKWS1
Known GenesFAM203A, MROH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982291
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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