A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137689



Internal ID19247869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:52411557..52489257hg38UCSC Ensembl
OuterchrX:52154700..52232400hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3877701
hg1977701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990189
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137689
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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