A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151194



Internal ID19200653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155027971..155028056hg38UCSC Ensembl
OuterchrX:154256246..154256331hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002129
SamplesKWB1
Known GenesFUNDC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151194
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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