A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139445



Internal ID19276001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10233099..10233448hg38UCSC Ensembl
OuterchrY:10070708..10071057hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960474, nssv3976360
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139445
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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