A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv336n106



Internal ID20159693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1495591..1495708hg38UCSC Ensembl
chr10:1537786..1537903hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121088, nsv1144614, nsv1134974
SamplesKWS1, KWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv336n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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