A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609183



Internal ID20982254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26928747..26929114hg38UCSC Ensembl
chr7:26968366..26968733hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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