A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv307n106



Internal ID22794135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240207600..240208500hg38UCSC Ensembl
chr1:240370900..240371800hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118150, nsv1121794
SamplesKWS2, KWS1
Known GenesFMN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv307n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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