A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608277



Internal ID20981348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31504276..31523917hg38UCSC Ensembl
chr7:31543890..31563531hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3819642
hg1919642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156031
Samples
Known GenesCCDC129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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