A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv63n100



Internal ID20151679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16583102..16956580hg38UCSC Ensembl
chr1:16909597..17283075hg19UCSC Ensembl
chr1:16782184..17155662hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38373479
hg19373479
hg18373479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006276, nsv1011167, nsv1006712, nsv1012813, nsv999319, nsv1004375, nsv1002264, nsv1005462, nsv1008466, nsv1013560, nsv1002158, nsv1012664, nsv1013554, nsv1003788, nsv1015052
Samples
Known GenesCROCC, CROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv63n100
Frequency
Sample Size29084
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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