A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527502



Internal ID20900863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74748230..74754036hg38UCSC Ensembl
chr17:72744369..72750175hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg385807
hg195807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038441
Samples
Known GenesMIR3615, SLC9A3R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527502
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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