A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615674



Internal ID20988745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115514914..115536912hg38UCSC Ensembl
chr7:115154968..115176966hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3821999
hg1921999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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