A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604474



Internal ID20977545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100441064..100447543hg38UCSC Ensembl
chr7:100038687..100045166hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386480
hg196480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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