A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126953



Internal ID19279420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:153201986..153230686hg38UCSC Ensembl
OuterchrX:152434700..152463400hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828701
hg1928701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4324n106
Supporting Variantsnssv3985236
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126953
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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