A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604555



Internal ID20977626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2772523..2773499hg38UCSC Ensembl
chr7:2812157..2813133hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157043
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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