A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121976



Internal ID18908860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:33087094..33088894hg38UCSC Ensembl
Outerchr19:33578000..33579800hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969399
SamplesKWS2
Known GenesGPATCH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121976
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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