A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997544



Internal ID19188743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40645932..40646265hg38UCSC Ensembl
OuterchrX:40505184..40505517hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148760
Supporting Variants
SamplesKWB1
Known GenesCXorf38
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997544
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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