A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078699



Internal ID19318093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1403306..1407407hg38UCSC Ensembl
chrY:1472199..1476300hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg384102
hg194102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762004
SamplesKWP1
Known GenesASMTL, ASMTL-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078699
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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