A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122270



Internal ID18907178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151906928..151919028hg38UCSC Ensembl
OuterchrX:151075400..151087500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812101
hg1912101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969717
SamplesKWS2
Known GenesMAGEA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122270
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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