A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611499



Internal ID20984570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65664001..65910200hg38UCSC Ensembl
chr7:65128948..65375187hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38246200
hg19246240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6874n223
Supporting Variantsnssv18225415
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, VKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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