A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4168n106



Internal ID22797996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135906754..135907854hg38UCSC Ensembl
chr9:138798600..138799700hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1122249, nsv1126928
SamplesKWS2, KWS1
Known GenesCAMSAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4168n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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