A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606752



Internal ID20979823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155267584..155271284hg38UCSC Ensembl
chr6:155588718..155592418hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383701
hg193701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139773
Samples
Known GenesCLDN20, TFB1M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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