A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967232



Internal ID19242401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3061902..3062602hg38UCSC Ensembl
Outerchr19:3061900..3062600hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136268
Supporting Variants
SamplesKWS2
Known GenesAES
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967232
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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