A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139402



Internal ID18933936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:48908216..48908279hg38UCSC Ensembl
OuterchrX:48765493..48765556hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976989
SamplesKWS2
Known GenesSLC35A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139402
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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