A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516219



Internal ID20889580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63873618..63918780hg38UCSC Ensembl
chr17:61950978..61996140hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3845163
hg1945163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3218n223
Supporting Variantsnssv18037782
Samples
Known GenesCSH1, CSH2, CSHL1, GH1, GH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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