A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516995



Internal ID20890356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74852442..74854901hg38UCSC Ensembl
chr17:72848581..72851040hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382460
hg192460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038447
Samples
Known GenesGRIN2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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