A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972221



Internal ID18885933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:13806143..13806199hg38UCSC Ensembl
Outerchr19:13916957..13917013hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123222
Supporting Variants
SamplesKWS2
Known GenesZSWIM4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972221
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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