A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037692



Internal ID20604732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7678101..7683300hg38UCSC Ensembl
chr17:7581419..7586618hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510179
Supporting Variants
Samples
Known GenesTP53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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