A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976592



Internal ID19232477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10205516..10205584hg38UCSC Ensembl
OuterchrY:10043125..10043193hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124536
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976592
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer