A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075349



Internal ID19321184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1408306..1410207hg38UCSC Ensembl
chrY:1477199..1479100hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772694
SamplesKWP1
Known GenesASMTL, ASMTL-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075349
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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