A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3630864



Internal ID12131004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38541289..38541340hg38UCSC Ensembl
chr7:38580889..38580940hg19UCSC Ensembl
chr7:38547414..38547465hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1768159
Supporting Variants
SamplesHuRef
Known GenesAMPH
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3630864
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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