A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126962



Internal ID19276504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:15289220..15294920hg38UCSC Ensembl
OuterchrY:17401100..17406800hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985246
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126962
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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