A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4316n106



Internal ID22798144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149938682..149939782hg38UCSC Ensembl
chrX:149106900..149108000hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119645, nsv1133772
SamplesKWS2, KWS1
Known GenesLINC00894
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4316n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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