A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601471



Internal ID20974542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160428487..160466600hg38UCSC Ensembl
chr6:160849519..160887632hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3838114
hg1938114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139859
Samples
Known GenesLPAL2, SLC22A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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