A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601248



Internal ID20974319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120273001..120273700hg38UCSC Ensembl
chr7:119913055..119913754hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153652
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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