A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978814



Internal ID19241389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:23523353..23558753hg38UCSC Ensembl
OuterchrY:25669500..25704900hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3835401
hg1935401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140103
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978814
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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