A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641007



Internal ID7027781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63848706..63849774hg38UCSC Ensembl
Innerchr17:63848706..63849774hg38UCSC Ensembl
Outerchr17:63848441..63850057hg38UCSC Ensembl
chr17:61926066..61927134hg19UCSC Ensembl
Innerchr17:61926066..61927134hg19UCSC Ensembl
Outerchr17:61925801..61927417hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15722588, essv15722591, essv15722587, essv15722589, essv15722590
SamplesNA18967, HG00705, HG02190, HG00620, HG00593
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641007
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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