A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527256



Internal ID20900617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73553754..73581029hg38UCSC Ensembl
chr17:71549893..71577168hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3827276
hg1927276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038373
Samples
Known GenesSDK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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