A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601679



Internal ID20974750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65055051..65888939hg38UCSC Ensembl
chr7:64515429..65353926hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38833889
hg19838498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6860n223
Supporting Variantsnssv18158607
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, VKORC1L1, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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