A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990201



Internal ID19232628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155560539..155569939hg38UCSC Ensembl
OuterchrX:154790200..154799600hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg389401
hg199401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137701
Supporting Variants
SamplesKWS2
Known GenesTMLHE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990201
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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