A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665919



Internal ID9932024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97764306..97789483hg38UCSC Ensembl
chr7:97393618..97418795hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825178
hg1925178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6510272, essv5986320, essv6184753, essv5441408, essv5815524, essv6584587, essv6537780, essv6596886, essv5458380
SamplesHG00403, NA19719, HG00577, HG01095, HG00651, HG00704, HG00267, HG00343, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665919
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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