A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146576



Internal ID20713616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56982640..57007032hg38UCSC Ensembl
chr6:56847438..56871830hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3824393
hg1924393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401739
Supporting Variants
Samples
Known GenesBEND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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