A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606257



Internal ID20979328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117573101..117574800hg38UCSC Ensembl
chr7:117213155..117214854hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148663
Samples
Known GenesCFTR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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