A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001672



Internal ID19194562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:29099..42300hg38UCSC Ensembl
OuterchrY:29099..42300hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3813202
hg1913202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148161
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001672
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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