A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982118



Internal ID12627785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28724519..30687025hg38UCSC Ensembl
Innerchr15:28969665..30979228hg19UCSC Ensembl
Innerchr15:26768706..28766520hg18UCSC Ensembl
Innerchr15:26768706..28766520hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381962507
hg192009564
hg181997815
hg171997815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751526
Supporting Variants
SamplesBEC_521
Known GenesAPBA2, ARHGAP11B, CHRFAM7A, DKFZP434L187, FAM189A1, GOLGA6L7P, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC100289656, LOC101059918, LOC646278, NDNL2, TJP1, ULK4P1, ULK4P2, ULK4P3, WHAMMP2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982118
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer