A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612922



Internal ID20985993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12644740..12645044hg38UCSC Ensembl
chr7:12684365..12684669hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152588
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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