A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115897



Internal ID19263965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120343645..120350345hg38UCSC Ensembl
OuterchrX:119477500..119484200hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg386701
hg196701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978459
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115897
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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