A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513187



Internal ID20886528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:764805..895609hg38UCSC Ensembl
chr17:668045..798849hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38130805
hg19130805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038234
Samples
Known GenesGLOD4, NXN, RNMTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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