A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610802



Internal ID20983873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65063205..65752770hg38UCSC Ensembl
chr7:64523583..65217757hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689566
hg19694175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6860n223
Supporting Variantsnssv18158609
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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