A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141929



Internal ID20708969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156976501..156982100hg38UCSC Ensembl
chr6:157297635..157303234hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614774
Supporting Variants
Samples
Known GenesARID1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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