A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4324n106



Internal ID22798152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153201886..153230686hg38UCSC Ensembl
chrX:152434700..152463500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828801
hg1928801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1133774, nsv1126953
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4324n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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