A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124491



Internal ID19261799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2917943..2918006hg38UCSC Ensembl
OuterchrX:2835984..2836047hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975786, nssv3959310
SamplesKWS2, KWS1
Known GenesARSD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124491
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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