A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4037n106



Internal ID20163394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63767866..63844166hg38UCSC Ensembl
chr9:68363600..68439900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3876301
hg1976301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115825, nsv1129037
SamplesKWS2, KWS1
Known GenesLOC642236
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4037n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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