A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415071



Internal ID21072624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70425868..70427249hg38UCSC Ensembl
chr6:71135571..71136952hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381382
hg191382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144444
Samples
Known GenesFAM135A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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