A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601835



Internal ID20974906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29018048..29655876hg38UCSC Ensembl
chr7:29057664..29695492hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38637829
hg19637829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229741
Samples
Known GenesCHN2, CPVL, LOC646762, PRR15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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