A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982384



Internal ID19215958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:328065..329465hg38UCSC Ensembl
OuterchrY:238800..240200hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145296
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982384
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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