A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2861n106



Internal ID22796689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97433139..97438062hg38UCSC Ensembl
chr4:98354290..98359213hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135367, nsv1130486
SamplesKWS2
Known GenesSTPG2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2861n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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