A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615300



Internal ID20988371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17503136..17606306hg38UCSC Ensembl
chr7:17542760..17645930hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38103171
hg19103171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6604n223
Supporting Variantsnssv18152967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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