A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3703n106



Internal ID20163060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152401015..152416415hg38UCSC Ensembl
chr7:152098100..152113500hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3815401
hg1915401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110501, nsv1115763
SamplesKWS1, KWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3703n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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