A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035267



Internal ID20602307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38351401..38352400hg38UCSC Ensembl
chr17:36507284..36508283hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499649
Supporting Variants
Samples
Known GenesSOCS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.04921


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