A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987591



Internal ID19203858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:529065..570365hg38UCSC Ensembl
OuterchrY:439800..481100hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3841301
hg1941301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132800
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987591
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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