A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960295



Internal ID19224677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:5606459..5612659hg38UCSC Ensembl
OuterchrY:5474500..5480700hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg386201
hg196201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110640
Supporting Variants
SamplesKWS1
Known GenesPCDH11Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960295
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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