A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3700n106



Internal ID20163057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152277715..152286615hg38UCSC Ensembl
chr7:151974800..151983700hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg388901
hg198901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119237, nsv1139911
SamplesKWS1, KWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3700n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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