A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115265



Internal ID19267309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:53138489..53138568hg38UCSC Ensembl
OuterchrX:53167671..53167750hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992580, nssv3960436
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115265
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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