A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149985



Internal ID18854476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:115651735..115666622hg38UCSC Ensembl
OuterchrX:114886055..114900942hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3814888
hg1914888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998772
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149985
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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