A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604112



Internal ID20977183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44377915..44379919hg38UCSC Ensembl
chr7:44417514..44419518hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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