A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958397



Internal ID19208099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:95795853..95796481hg38UCSC Ensembl
OuterchrX:95050852..95051480hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109950
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958397
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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