A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3648n106



Internal ID20163005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114313446..114313758hg38UCSC Ensembl
chr7:113953501..113953813hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130136, nsv1121386
SamplesKWS2, KWS1
Known GenesFOXP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3648n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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