A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3370n106



Internal ID22797198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119096337..119096666hg38UCSC Ensembl
chr6:119417502..119417831hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1140688, nsv1127797
SamplesKWS2, KWS1
Known GenesFAM184A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3370n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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