A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126138



Internal ID19259325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44531292..44531399hg38UCSC Ensembl
OuterchrX:44390538..44390645hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984346
SamplesKWS1
Known GenesFUNDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126138
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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