A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1772n106



Internal ID19019881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35105883..35105942hg38UCSC Ensembl
chr19:35596787..35596846hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119470, nsv1140147
SamplesKWS1, KWS2
Known GenesHPN-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1772n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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