A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133774



Internal ID19257565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:153201886..153230586hg38UCSC Ensembl
OuterchrX:152434800..152463500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828701
hg1928701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4324n106
Supporting Variantsnssv3969349
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133774
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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