A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078697



Internal ID19322371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:978264..998865hg38UCSC Ensembl
chrY:888999..909600hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3820602
hg1920602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770141
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078697
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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