A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959833



Internal ID19210245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:17388720..17400820hg38UCSC Ensembl
OuterchrY:19500600..19512700hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3812101
hg1912101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119392
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959833
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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