A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141074



Internal ID19248827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103524104..103554274hg38UCSC Ensembl
OuterchrX:102779032..102809202hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3830171
hg1930171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992588
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141074
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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