A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740976



Internal ID15085582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61393195..61393211hg38UCSC Ensembl
Innerchr1:61393194..61393212hg38UCSC Ensembl
Outerchr1:61393145..61393261hg38UCSC Ensembl
chr1:61858867..61858883hg19UCSC Ensembl
Innerchr1:61858866..61858884hg19UCSC Ensembl
Outerchr1:61858817..61858933hg19UCSC Ensembl
chr1:61631455..61631471hg18UCSC Ensembl
Innerchr1:61631472..61631454hg18UCSC Ensembl
Outerchr1:61631405..61631521hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38975
hg19975
hg18975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3339821
Supporting Variants
SamplesNA19240
Known GenesNFIA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740976
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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