A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142719



Internal ID19273239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56829871..56830039hg38UCSC Ensembl
OuterchrY:58976018..58976186hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994206
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142719
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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