A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136262



Internal ID18923989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:719900..720600hg38UCSC Ensembl
Outerchr19:719900..720600hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1677n106
Supporting Variantsnssv3989876
SamplesKWS2
Known GenesPALM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136262
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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