A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3705n106



Internal ID20163062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152408937..152408996hg38UCSC Ensembl
chr7:152106022..152106081hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1140862, nsv1132101
SamplesKWS1, KWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3705n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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