A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610960



Internal ID20984031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6917582..7304563hg38UCSC Ensembl
chr7:6957213..7344194hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38386982
hg19386982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6557n223
Supporting Variantsnssv18227057
Samples
Known GenesC1GALT1, LOC100131257, LOC101927354
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610960
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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