A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972220



Internal ID18897423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:11525806..11525870hg38UCSC Ensembl
Outerchr19:11636621..11636685hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123221
Supporting Variants
SamplesKWS2
Known GenesECSIT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972220
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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