A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964674



Internal ID19227497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10206638..10206774hg38UCSC Ensembl
OuterchrY:10044247..10044383hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111766
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964674
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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