A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531135



Internal ID20904496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48892469..48900915hg38UCSC Ensembl
chr17:46969831..46978277hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg388447
hg198447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036086
Samples
Known GenesATP5G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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