A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145280



Internal ID19263922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2500459..2501359hg38UCSC Ensembl
OuterchrX:2418500..2419400hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982368
SamplesKWS1
Known GenesDHRSX, ZBED1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145280
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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