A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604472



Internal ID20977543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7704901..7707600hg38UCSC Ensembl
chr7:7744532..7747231hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158350
Samples
Known GenesRPA3, RPA3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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