A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606714



Internal ID20979785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65038637..65873563hg38UCSC Ensembl
chr7:64499015..65338550hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38834927
hg19839536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6860n223
Supporting Variantsnssv18158606
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, VKORC1L1, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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