A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4302n106



Internal ID22798130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139963637..139963770hg38UCSC Ensembl
chrX:139045796..139045929hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1128412, nsv1115297
SamplesKWS2, KWS1
Known GenesCXorf66
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4302n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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