A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217869



Internal ID20784909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34153819..34161340hg38UCSC Ensembl
chr6:34121596..34129117hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387522
hg197522
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400035
Supporting Variants
Samples
Known GenesGRM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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