A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614254



Internal ID7001149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98327308..98335152hg38UCSC Ensembl
Innerchr7:98327308..98335152hg38UCSC Ensembl
Outerchr7:98327280..98335170hg38UCSC Ensembl
chr7:97956620..97964464hg19UCSC Ensembl
Innerchr7:97956620..97964464hg19UCSC Ensembl
Outerchr7:97956592..97964482hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387845
hg197845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12905058
SamplesHG01954
Known GenesBAIAP2L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614254
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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