A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395776



Internal ID21053329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53695408..53696120hg38UCSC Ensembl
chr6:53560206..53560918hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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