A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765987



Internal ID19308243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11250230..11250283hg38UCSC Ensembl
chrY:13405906..13405959hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076300
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765987
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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