A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075758



Internal ID19320400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20093884..20191267hg38UCSC Ensembl
chrY:22255770..22353153hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3897384
hg1997384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771331
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075758
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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