A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498986



Internal ID20872201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1428801..1430500hg38UCSC Ensembl
chr17:1332095..1333794hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034376
Samples
Known GenesCRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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