A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138514



Internal ID337698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13415636..13416671hg38UCSC Ensembl
chrY:15527516..15528551hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738427
Samples
Known GenesUTY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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