A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109950



Internal ID19253106
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 StatusM
Merged Variantsdgv4269n106
Supporting Variantsnssv3958397
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109950
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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