A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4318n106



Internal ID20163675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150983327..150984927hg38UCSC Ensembl
chrX:150151800..150153400hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1113046, nsv1126951
SamplesKWS2, KWS1
Known GenesHMGB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4318n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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