A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976361



Internal ID19243528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11250231..11250283hg38UCSC Ensembl
OuterchrY:13405907..13405959hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115312
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976361
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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