A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527951



Internal ID20901312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63957876..63986846hg38UCSC Ensembl
chr17:62035236..62064206hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3828971
hg1928971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037742
Samples
Known GenesSCN4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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