A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500234



Internal ID20873459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39242355..39242784hg38UCSC Ensembl
chr17:37398608..37399037hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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