A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610427



Internal ID20983498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124572259..124572672hg38UCSC Ensembl
chr7:124212313..124212726hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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