A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504916



Internal ID20878180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7187304..7189207hg38UCSC Ensembl
chr17:7090623..7092526hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381904
hg191904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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