A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497570



Internal ID20870777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10071005..10075753hg38UCSC Ensembl
chr17:9974322..9979070hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg384749
hg194749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033988
Samples
Known GenesGAS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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