A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3586n106



Internal ID20162943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71602815..71604415hg38UCSC Ensembl
chr7:71067800..71069400hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115752, nsv1110487
SamplesKWS1, KWS2
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3586n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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