A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990211



Internal ID19244373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:4027359..4032559hg38UCSC Ensembl
OuterchrY:3895400..3900600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137710
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990211
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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