A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137171



Internal ID19285555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56829955..56851308hg38UCSC Ensembl
OuterchrY:58976102..58997455hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3821354
hg1921354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4370n106
Supporting Variantsnssv3975858
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137171
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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