A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978424



Internal ID19243010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:864965..933565hg38UCSC Ensembl
OuterchrY:775700..844300hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3868601
hg1968601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140088
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978424
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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