A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610772



Internal ID20983843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119384483..120677013hg38UCSC Ensembl
chr7:119024537..120317067hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg381292531
hg191292531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222263
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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