A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610317



Internal ID20983388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43815124..43821614hg38UCSC Ensembl
chr7:43854723..43861213hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg386491
hg196491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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