A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505881



Internal ID20879154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33631865..33632445hg38UCSC Ensembl
chr17:31958884..31959464hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035021
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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