A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513908



Internal ID20887257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39722075..39722596hg38UCSC Ensembl
chr17:37878328..37878849hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035370
Samples
Known GenesERBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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