A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113054



Internal ID19251079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:23151353..23156653hg38UCSC Ensembl
OuterchrY:25297500..25302800hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967948
SamplesKWS2
Known GenesDAZ1, DAZ4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113054
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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